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REPUBLIQUE DE
VANUATU
JOURNAL OFFICIEL
nECE!VEO JUL 1 1 j988
REPI)BLle OF
VANUATU
OFFCIAL GAZETTE
) 27 JUIN 1988 GAZETTE EXTRAORDINARY
NUMERO SPECIAL 27 JUNE. 1988
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SONT PUBLIES LES TEXTES SUIVANTS
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LOI NO. 9 DE 1988 PORTANT MODIFI- ! CATION DU P~GLEMENT CONJOINT ! RELATIF A LA VENTE DE MEDICM4ENTS ! (INTERDICTION) . !
ARRETES , , r , !
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NOTIFICATION OF PUBLICATION
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THE JOINT SALE OF MEDICINES (PROHIBITION) (AMENDMENT) ACT NO. 9 OF 1988.
ORDERS
THE SALE OF MEDICINES (REGULATION) ORDER NO. 25 OF 1988.
THE FIREARMS REGULATIONS NO. 27 OF 19~8.
THE FIFlliARMS ACT NO. 7 OF 1987 -NOTICE
REPUBLIC OF VANUATU ___ .·_,~n __ ~ , .•• ,_,_. ___ ~. __ ~~.
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Arr.endment of secLion 2 of the Joint Regulation No. 32 of 1966.
2. Insertion of section 2A in the Regulation.
3. Amendrr.ent of section 3 of the Regulation.
) 4. COffiUi.eOCement.
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REPUBLIC OF VANUATU __ .n _~_, •• __ ,_,, __ .~ __ . __ ~ ••• ~_
Assent: 12.4.88 Commencement: 27.6.88
An Act to arr,end the Joint Sale of Medici.nes (ProhlbiClon) Regulation No.32 of 1966.
BE IT ENACTED by the President and Parliament as follows;-
AMENDMENT OF SECTION 2 OF THE JOINT REGULATION No. 32 OF 1966 1. Section 2 of the Joint Sale of Medicines (Prohibition) Regulation No.
32 of 1966 (in lha ACL referred to as the "Regulation") is amended by the repeal of subsections (3) and (4) of that section.
INSERTION OF SECTION 2A IN THE REGULATION 2. The following section is inserted after section 2 of the Regulation;
"REGULATION 2A. (1) The i'1inisLer may by order rr,ake regulations not inconsistent
with the provisions of this Regulation -
(a) regulating the sale of medicines. or
(b) prohibiLing the sale of any medicines except upon the prescription of a medical practitioner or dental practitioner Ol- veterinary surgeon.
(2) Any regulation made under subsecr.ion (1) <T,ay authorize the Principal Pharmacist to rr.ake and issue notices or directives with respect to such matters prescribed by that regulation."
AMENDMENT OF SECTION 3 OF THE REGULATION ----- 3.--Section 3-of the Regulation is arr.ended by the repeal of subsection(l)
of that section and the SubSLitution therefor of the follOWing subsection;
"(1) No person shall sell wholesale any rr,ediclne other than those as rr.ay be prescribed under section 2A(1) to any person other than a pharrriacisl or druggist."
COMMENCEMENT 4. This Act shall come into force on the date of its publication in the
Gazette.
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1.91 NO. 9 DE 1988 POl!.TANT rlODIFICATION DU. P>EGLEHENT CONJOINT
I@LATIF A LA VENTE DE IIJEDICAfJiENTS (INTEPJ)ICTIOl])
Sommaire
r~odification de l'Article 2 du Reglement Conjoint No. 32 de 1966.
Insertion de l'Article 2A dans Ie Reglement.
Modification de 1 'Article " c1u Reglement. ;;
gntree en vigueuro
REPUBLIUUE DE VilNUATU
LOI NO.9 l;E 1938 PORTANT HODIFICATION DU REGLEJI'lENT
CONJOINT RELATIF A LA VENTE DE MEDICflHli\1'L'l:§:
(INTERDICUQN)
portant modification du Reglement Conjoint No. 32 de 1966 relatif 2\ la vente de medicaments tinterdiction)
1e president de la Hepublique et Ie Pal'lement promulguent 1etexto suivant g
I'lODIFICATION DE L' ARTICLE 2 DU IillGLEJ:1ENT CONJOINT NO. 32 DE 1966 1. L'article 2 du l1eglement Conjoint No. 32 de 1966 relatif a 10.
vente de medicamonts (interdiction) (mentionne dons. 10. presente 10i comme "Reglement li ) est modifie par la suppression des paragraphes (3) ot (I.f) dudit articlo.
INSERTION DE L' ART I CIJ": 2A DilNS L)3; REGLEJI'lENT 2. L'article suivant est ins ere apres l'o.rticle 2 du Reglement g
"HEGLE 2A. 1) Le Ministre peut prendre des ordonnances fixant des
l'egles compatibles avec les dispositions du present l1eglement g
0.) reglementant :La vente de medicaments, ou
b) interdisant 10. vente de tout medicament oauf sur ordonnance d'un ,11odecin, d'un dentiste au d'un chiru1'gien veterinai1'e.
2) Toute ordonnance prise conformement au paragraphe 1) du<1i t article peut habili tel" le pha1'macien principal a rencl1'e ot a lJublier des notes ou directives concernant 1es-questions prosc1'ites par Iadite regIe".
MODIFICATIOl'! DE L' fillTICLE 3 DU RI~GLEJ:mN'l' 3. L'article;;' du Regloment est modifie pn1' 10. suppression du pal'a
graphe 1) dudit article et par son remplacement par 1e paragraphe suivant g
"1) Nul no pout venclre des mec1.icaments en gros a l'exception de c etL'C pouvant etre prosc1'i ts Gonformement a 1 t article 2/1 1) El -coute personne autre qu 'un pharmacien ou un deposi taire de r:ledic aments i' •
ENTTlJi$ EN VIGUEUH. '-1.. La presente Loi entrera en vigueur Ie jour de sa publication
au Journnl officie1.
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THE SALE OF MEDICINES (REGULATION) ---·'-'--ORDER-No'.-25 oFT9Sif'-----
An Order to regulate the sale of medicines.
IN EXERCISE of the powers conferred by Section 2A of the Joint Sale of eledicine5 (Prohibition) Regulation No.n of 1966. as amended, 1 hereby tT,ake the followln:; regulations:.
INTERPRETATION 1. In these regulalions unless the context otherwise requires;
"Ch ild .. resistant c losure H IT,eans;
(a) a closure which is resistant to opening by children,
(b) in the case of a can fitted with a pres-on lid, a lid of the design known as "double tight" or "tripple tight",
"dosage unit li I)',eans an individual dose of a rr,edicine and includes a tablet, capsule, cachet, single dose powder or single dose sacheL of powders or granules
"internal use ll means administra,tion:
(a) orally, except for topical effect in the mouth. or
(b) fo·r absOrptl0n and the production of a systemic effect,
(0 by way of a body orifice other than the mouth. or
(ii) parenterally. other than by appllcatlon to unbroken skin,
Hmedicine" means any substance or preparati.on which is included in [hie;
.Schedules to this Order;
IIprimary pack" ",eans the pack in which a rr,edicine and its irrt1TLe.d.ia~.e
container or i,mmediate wrapper or measure pack are presented for sale or supply.
(a) "imrr,ediale container" includes all forq,s of containers in which a medicine is directly packed bUl doe.s not incl1.lde any such containe r in.tended for consumption or any immediate wrapper,
(b) "imlT,ediate wrapper" means 'I.etal foil., plastic foil, waxed paper, or any sucb material not intended for consulT.ption, when used as the first wrapper for a dosage unit which contains any medicine;
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(c) "rr,easure pack' means one of two or more sealed containers each of which contains a ffieasured quantity of medicine for use on one occasion as a pesLici,de and "hich forIT, part of a single primary pack.
"t herapeut ic use ll rr,eans use in or in connection w.i th I
(a) the prevenllng, diagnosing, cur tng or alleviating of a disease, ai Iment, defect or injury in hurr.an beings or aniITlals 1
(b) the influencing" inhibiting or IT,odifying of a physiological process in hUIT,an beings or animals~ or
(c) the cestIng of the suscept ibllity of human beings or animals to a disease or ailment;
"topical use" means application. of ,a 'f,edicine for the purpose of producing a localised effect on the surface of the organ or "ith1n the issue to which j t is appUed.
SALE OF MEDICINES 2,'(1)' Any p'e'rson IT,ay sell any of, the ',,:ediclnes specified in Schedule 1
her'eto~-
(2) No person, other than a p"errr,acist or a dtuggist, shall sell any of the medicines specified in Schedule 2 hereto,
(3 )
NOTICES 3. (1)
No person shall sell the medicines specified except upon the prescription of a medical practitioner or a veterinary surgeon.
in Schedule 3 hereto, practitioner, dental
The Principal Pharmaclst may issue such notices as he deems fit for the proper carrying out of these regulations.
(2) Any notice issued under this regulation shall be publisbed in tbe Official Gazette.
COMMENCEMENT 4. This Order shall come inl.o force on the date of its publication in tbe
" Gazette,
MADE at Port Vila, this 28th day of June
FRED TIMAKATA Minister 'O.fiieiiith
, 1988.
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[ . SCHEDULE 1
ACETIC ACID (excluding its salts and derivatives) and preparations containing ".ore than 80 per cent of acetic acid, for therapeutic use.
ALOXIPRIN
AMMONIATED MERCURY
ANTAZOLINE in eye drops.
ASPIRIN ,,>:c:.:.e~~
(a) when included in Schedule ·3,
(h) in lndividually wrapped powders or sachets of containing 650 milligrams or less of aspirin therapeUtlCally aCtlVe cons[icuent when;
gnmules each as· [he on1 y
[he pack is labelled wi th the wa rn ing stateff.ent:
WARNING - TlllS MEDJ CATlON ["lAY BE DANGEROUS WHEN USED IN LARGE AMOUNTS OR FOR A LONG PERIOD. or
CAUTlON - THISPREPARATlON IS FOR THE RELIEF OF HINOR AND TEdPORAt~Y AILNENTS AND· SHOULD llE USED STRICTLY AS DIRECTED. PROLONGED USE WiTHOUT l'JEDlCAL SUPERVISION COULD BE HAl<HFULi and
(ii) in a primary pack contaimng not more than 12 such powders or sacbets of granules, or
(c) tablets or capsules each containing 325 rr,illigrarr,s or less of aspi.rin as the only therapeutically active constituent when:
(1) the pack is labelled with the warning statement:
~JARNING - THIS HED1CATlOI~ HAY BE DANGEROUS WHEN USED IN LARGE AP.lOUNTS OR FOR A LONG PERlOD: or
CAUTlON - THIS PREPARATION IS FOJ{ THE RELlEr' OF i-IINOR AND TENPORARY AI Li'lENTS AND SHOULD BE USED STRICTLY AS DH<ECTED. PROLONGED USE IvIIHOUT HEDICAL SUPERVISION
J COULD BE HARJVJFUL; and
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(U) packed in blister or strip packaging or in containers with a child-resistant closure. and
(iii.) in a prirr,ary pack containing not rr,ore than 25 such tablets or capsules.
ATROPINE, """:,,,e~ atropine methonitrate included in Schedule 3,
(a) in preparations containing 0.25 per cent or less of atropine; or
(b) acrol'ine sulphate, 0.6 mg tablets in packs of six. when labelled for treatment of organophosphorus poisoning.
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BELLADONNA in preparations containing 0_25 per cent or less ofche alkaloids of belladonna, calculated as hyoscyamine.
BENZAMINE when included In;
(a) lozenges, pasulles, tablets or capsules cOntainlng 30mg or less of benzaffiine, in eachi
(b) suppositories or bougies contalning 20Qrr,g or less of benza'l'oine in each,; or
(c) preparations for exter.nal use, ocher chan eyedrops, containing 10 per cent or less of benzamine.
BENZOCAINE when included in;
(a) lozenges, pastilles, tablets or capsules containing 30mg or less of benzocaine in each;
(b) suppositories or bougies containing 200mg or less of benzocaine in each.~ or
(e) prepar.ations for external use, other than eye drops, containing 10 per cent or less of benzocaine.
BENZOYL PEROXIDE in preparaLions for external. hurr,an therapeut Ic use containing 5 per cent or less benzoyl peroxide.
BENZYDAMINE in preparations for toplcal use containing 3 per cent or less of :;enzydamine.
BROl~HF.XINE
BROMPHENIRAMINE when carr,pounded with one or rr,are of the following tT,edicarr,enls,
. (a) an antitussive ~~<::"e~ codeine or dihydrocodeine.,
(b) an expectorant. or
(e) a sy~patho~imetic amine,
~!,('."p~ in preparations for the trealrr,ent of children under 2 years of age;
BUCLIZINE 1n pritT,ary packs of 10 d<)ses or less, for the prevention or treatment of !I-,ot.ion sickness.
BUTYLAMINOBENZOATE when included in;
(a) lozenges. pastilles, tablets or capsules containing 30 mg or less of butylarrlinoben-zoate in each;
(b) suppositories or bougies containing 20Qrr,g or less of butylami nobenzoate in each~ or
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(c) preparations for external use, other than eye, drops, containing 10 per cent or: less of butylaminobenzoate.
CARBARYl. in prepa"alions for external huq,an therapeutic use containing 2 per cent or less of carbaryl.
CARBENOXOLONE for toplcal oral use.
CARBETAPENTANE <;l<c:"p.t in preparations containing 0.5 per cent or less of carbetaiJentane.
CHLOROFORM in preparations for therapeutic use "xc;e,l'i;.
(a) I,hen included in Schedule 3, or
(b) in preparations containing 0.5 per cent or less of chloroform.
CHLORPHENlRAMINE when compounded with one or more of the following medica1f,ents:
(a) an antitusslve "l<C:"p'~ codelne or dihydrocodeine,
(b) an expectorant" or
~~xce..i~t in preparaLlons for the treatIT,ent of children under 2 years of age.
CINNAMEDRINE
CLIOQUINOL and oLher halogenated derivatives of 8-Hydroxyquinoll.ne for external h\.;f(,an use.
CODEINE
(a)' when corr,pounded with aspirin, paracetamol or salicylamide or any one of their derivatives, in tablets or capsules each containing 10q,g or less of codeine, and no other analgesiC substance, when,
(i) packed 111 blister or strip packaging or in COntainers with child-resistant closures, and
(ii) in a priq,aey pacit containing 25 or less dosage units; or
(b) when Coq,pounded with one or !r,ore other therapeutically accive substances:
(il in diVIded preparaUons comaining 10mg or less per dosage unit of codeine and with a reo%1f,ended dose not exceeding 15mg of codeine" or
(iil in undivided preparattons containing 0.25 per cent or less of codeine and with a recommended dose not exceeding 15rr,g of codelne.
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CREOSOTE, for therapeutic use, except in preparations containing 3 per cent or less of phenols included in SChedule"!.
CYANlDES - see hydrocyanic acid.
DDT . see dicophane.
DEXCHLORPHENIRAlHNE when corr,pounded with one or more of the following {r,edicarr,ent S ~
(a) an antitussive ~~~~e~ codeine or dihydrocodeine,
(b) an expectorant, or
(c) a sympatho!T,imetic amine~
~"~,,,p.! in preparations for the treatment of children under 2 years of age.
DEXTROMETHORPHAN when compounded with one or more other therapeutically active subs·tances in such a way that the dextromethorphan contained therein cannot be readily ext rae ted , when.
(a) in divided preflarations COntaIning 30mg or less per dosage unit and with a recorr,mended dose not exceeding 3Orr,g of dextromethorphan~ or
(b) in undivided preparati.ons contatnwg 0.3 per cent or less of dextrorr,et.horphan with a recoffimended dose not exceeding 3Orr,g of dext rOl.l,et,horphan.
DICOPHANE (DDT) in preparaLions for buman therapeutic use.
DICYCLOMINE i.n preparaLions containwg 0.1 per cent or less of dicyclomine.
DIMENHYDRINATE in prirr,ary pace.s of 1.0 doses or less, for tbe prevention or treatrrlent of rr.otion sickness.
DIMETHISOQUIN in preparations for topical use.
~_~DIPHEMANIL»ETHYLSULPHATE in preparat.10ns for topical use.
DIPHENHYDRAl!tINE
(a) in prirr,ary packs of 10 doses or less, for the prevention or t reat1Tlent of Tf,otion sickness 1 or
(b) when corr,pounded witb one or 'nore of tbe follOWing medicaments,
an anLiLussive e~~~e~ codelne or dibydrocodeine,
(ii) an expectorant. or
(iii) a sympat horr,i"cM~t i.e ami ne:
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':.~_~~e.£ in preparations for lhe tredL\T,enl of children under 2 years of age.
DIPHENYLPYRALINE \Vhen compounded with one or rr,ore of the fo11o\Ving me<!Jcarr,ents:
(a) an antitussive ~."!::'~J)t_ codeine or dihydrocodeine,
(b) an expectorant, or
c.::c:",!,r: in preparations for the treatIT,ent of children under 2 years of age.
DOXYLAMINE when tOIT,pounded with one or more of the following !i,edicaments:
(a) an antitussive ~xc:,:,IZ!. codelne ordhydrocodelne,
(b) an expectorant, or
':'''C:.''p'~ in preparations for the treatlT,ent of children under 2 years of age.
EPHEDRINE fOl- internal use, when cOlT,pounded with one or more other therapeuric-ally ac.live substances in preparations containing 30mgor lessol ephedrine per r.eCOtlHl,ended dose~ o~her than preparations for stilT,uiant. appetite suprla:s~Aon or tveighL control purposMe's:'-~~~~e~ in liquid pr,eparations 'containin'g 10rr,g or less of e phed ri ne pe r recorr,mended dose.
ERYTHRrfyL TETRANITRATE for therapeutic use.
2TAFEDlUNE
ETHER for Ll1e rapeut ie use ex~eel:::
(a) "hen included in Schedule 3, or
(b) in pr~paralions concaining 10 per cenl or less of ether.
ETHOHEPTAZINE in preparatins containing 1 per cent or less of ethoheptazine,
ETHYLMORPHINE, when cOlT,pounded with one or rr,ore other therapeutically active subst.ances:
(a) in divided p,"eparationscontaining 10mg or less per dosage unit and "i.th a recoIT,IT,ended dose not exceeding 15mg "fethylmorphine ~ or
(b) in undivided preparations containlng 0,25 per cent or ethylrr,orphine with a recolT,IT,ended dose not exceeding e thy lrr,o rph ine.
FLUORIDES for· hUIT,an therapeutic use:
less of 15rr.g of
(a) sodiUlTl f luoric..te \ or less of sodiu%
in preparaL lons for ingestion f luo ride pe r dosage unit, or
containing 2. 2mg
(b) in preparacions for toplcal use "~C:".f'!:.:
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GELSEMlUM
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(i) in dentifrices concaining 1000rr,g/kg or less of fluoride ion, or
(ii) in substances containing 15rr,g/kg or less of fluoride. ion.
GLUTARALDEHYDE for hurr,an therapeutic use.
GLYCERYL TRINlTRATE for cherapeullc use EO!':.':".!'!:. when included .in Schedule 3.
GUAIPHENESIN
( a)
(b)
in liquid preparations containIng 2 per cent (200 (f,g/lOrr,l) o.r less of guaiphenesln, or
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in divided preparations COntaining 120mg or less of gualphenesin in each dosage unit.
HEXACHLOROPHANE in preparations for tluman skin cleansing purposes containing 3 ,)er cent or I.ess. of hexachlorophane ".!':':!:.E.t in preparations for use on infants as specified in Schedule 3.
:;OHATROPINE in pr.cpJracions containing 0.25 per cent or less of horr,aeropine.
HUMAN CHORIONIC GONADOTROPHIN OR ANTIBODY in pregnancy test ilits.
EYDROCYANIC ACID and CYANIDES in preparations for therapeutic use containing the ,c(,u(valent of 0.15 per cent or less of hydrocyanic acid.
3 - HYDROXYQUINOLINE and ItS. non· halogenated de ri vat i ves for hU'f,an therapeut ic use, Qxcept in preparations for external use containing 1 per cent or less of s lIch s;b-s~!:-a-nces,
HYOSCINE, e'.'''.E!!':: hyoscine bULylbrorr,ide included in Schedule 3:
(a) in preparallons containing 0.25 per cent or less of hyoscine, 0["
(b) in transderrr,al applicators conLaining 2IT,g or less of hyoscine.
HYOSCYAMINE in preparaLi.ons containing 0.25 per cenl or less of hyoscyami ne.
HyOSCYAMUS in prep_arat ions conr.aini.ng 0,25 per cent or less of the alka loids of hyoscyamus calculated as hyoscyarr,ine,
IODINE (ellcludlng ics salts, derivaLLves and iodol'hors), in prparations for hurr,an therapeuti.c use containing IT,ore than 2.5 per cent of available iodlne.
IRON COMPOUNDS for human internal use e~"."t)l::
(a) when included in Schedule 3,
(b) in dividled preparations contaiOlng 5 mg or less of iron per dosage unit, or
(c) in liqUid oral preparations containing 0,1 per cent or less of lron.
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ISOPROPAHIDE in preparatlons conLaining 2 per cenc or less of isoproparr.ide for cutaneous use ..
ISOSORBIDE DINITRATE for therapeutic use.
LIGNOCAINE when included in;
(a) lozenges, pastilles, tablets or capsules containing 30mg or less of lignocaine in each;
(b) suppositories or bougies containing 20Orr.g or less of lignocaine in each. or
(c) preparations for external use. other than eye drops, con':aining 10 per cent or less of lignocaine.
LINDANE in preparations for excernal human therapeutic use containing 2 per cent or less of lindane.
LOBELIA in preparations cor,taining 0.5 per cent or less of lObeline, e_xc:~!'£ in ~H_"eparations for smoking or burning.
LUTEINISING HORMONE ANTIBODIES tn human ovulation test kits.
MALDISON in preparations for external hurr.an therapeutic use Containing 2 per cent or less of maldison.
HEBENDAZOLE for human therai)eut LC use.
ME:RCURIC CHLORIDE j n preparat cons con La [ning 0.5 per cent or less of rr.ercurIc chloride, "~."-~l"~ when included in a notice.
~IERCURIC IOIlHDE in preparal10ns for therapeutic use containlng 2 per cent or less of mercuric iodide.
i1ERCURIC NITRATE in prepartlOns for therapeutic use contalning 5 per cent or less of \T,ercuric nitrate~
MERCURIC OXIDE and all oXldes of mercury.
MERCURIC-POTASSIUM IODIDE in preparations containing the equivalent of 2 per cent or less -of rIiercuric iodide ~ in such fonT,.
MERCURY (metallic) for therapeutic use.
HERCURY ORGANIC COMPOUNDS for topical therapeutic use in preparaLions containing 0.5 per cent or less of mercury.
HETHOXAMINE "'~c::~l"~:
(a) preparaLlons containl.ng 0.5 per CenL or less of rr,ethoxamine, Of
(b) ,Jreparations for external use containing 1 per cent or less of methoxalJline .
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_'j. E:THOXYPHENAMINE
c;ETHYLEPHEDRINE
N APHAZOLINE
NICLOSAMIDE for hurr,an u,erapeutlc use.
NITRIC ESTERS of polyhydric alcohols for therapeutic use ~~c.~p~ when separately specified in these Schedules_
NOSCAPINE
OXETHAZAINE 1n preparations for interal use only_
OXOLAMINE
OXYMETAZOLINE PAPAVERINE
(a) when included in Schedule 3.
(b) in indiVidually wrapped powders or sachets of granules each containing 1000 rr,illigrams or less of paracetarr,ol as the only therapeutically active conSLituent when:
(1) the pack is labelled with the warning statement:
VlARNll~G - IHIS 11llDlCATION MY BE DANGEROUS WHEN USED IN LARGE A~lOUNTS OR FOR A LONG PERlOD, or
CAUTION -TEt'JPOHARY DIRECTED.
THIS PREPARATrON IS FOR THE RELIEF OF i1lNOR AND AILHENTS AND SHOULD BE nSED STRICTLY AS
PROLONGED USE ,HIHOUT aEDiCAL SUPERVlSION COULD BE. HARt'lFUL, and
(ii) in a pdmary pack containing not more than 12 such powders or sachets of granules; or
(c) tablets or' capsules each contdinlOg 500 milligrams or less of paracetarr,ol as the only therapeutically active constituent when;
(i) the pack is labelled wi th the' \Va rning statement:
,IARNING - THlS HED1CAll0N /!JAY BE DAl.GEROUS WHEN USED IN LARGE AtlOUNTS OR FOR A LONG PERIOD, or
CAUTLON -TEHPORARY DIRECTED.
THIS PREPARATION IS FOR THE RELIEF OF HINOR AND AILNENTS AND SHOULD BE USED STRICTLY AS
PROLONGED USE WITHOUT clEDlCAL SUPERVI SlON COULD BE HARl-lFUL, and
(ii) packed in blister or strip packaging or in containers with a Child-resistant closure, and
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PHEDRAZINE
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in a pri.mary ;>ack containing not rr,ore than 25 such tab lets 0 r capsule s.
PHENAMAZOLINE
PHENAZONE for external use,
PHENIRAMINE
(a) 1n primary packs of 10 doses or less, for the prevention or treatrr,ent of Illation sickness·, or
(b) when compounded with one or more of the following rr,edicaments;
(i) an andLussive ~"c.!!e!' codeine or dihydrocodeine,
(ii ) an expectorant; or
(ii i) a sympat hOtnilT,et. 1. c aTJ,i ne (,
except in preparar.ions for the Lreal'r,ent of chi1dren'~nder 2 yea'rs-of age.
PHENOL and any homologue of pr.enol balling below 220 C, for hurr,an therapeutic use, ~'!<:~e£ in preparcions containing 3 per cent or less by weight of such 5 ub stances.
PHENYLENEDIAMINES and a lkylatect pbeny lenedlarr,i nes for the rapeuL ic use,
PHENYLEPHRINE ~."c::."e!:
(a) when included in Schedule 3,
(b) preparations containlng 0.5 per cent or less of phenylephrine. or
(c) preparallons for external use containing 1 per cent or less of phenylephrine.
PHOLCODINE, when corr,pounded with one or more other therapeutically active substances:
(a) in divided prepartions containing 10mg or less ofpholcodine per dosage unit and with a recoa.mended dose not exceeding 25mg of pholeodine or
(b) in undivided preparations eont.ajning 0.5 per cent or less of pholcodine and with a reeoIT.IT,ended dose nct exceeding 25rr,g of pholcodine.
PODOPHYLLUM RESIN (podophylli n) for external human use in prepal'at lOS containing 10 per cent or less of podophyllin.
•• ,/10.
- 10 -
POTASSIUH CHLORATE for therafleutic use ~x.~~p!: in preparations containing 10 per cent or less of potassj.uffi chlorate.
PRA~JOXINE Vlben i neluded in preparallons for excernal use. olher than eye drops, concaining 1 per cent or less of pramoxine.
PROCYCLIDINE in preparaLlons contalncng 5 per cent or less of procyclldi,ne for cutaneous use.
PROMETHAZINE
(a) in primary packs of 10 doses or less. for the prevention or treatlTlent of motion sickness,! or
(b) when corr,pounded with one oc rr,ore of the following medicaments:
{iJ an an"tussive e.~~'CPt_ codeine or dlhydrocodelne,
(if ) an expectorant. or
(i ii)
~"~~P.t, in preparal ions for the t cealment of chi ldren unde r 2 yea,s of age.
PROPANTHELINE i.n preparations for toplcal use.
PROPYLHEXEDRINE in appllances for inhalation in whlch the substance is absorbed upon an inert solid material.
PSEUDOEPHEDRINE <;x"epr when included in Schedule 3:
(a) in divided preparaClons concaining 60rr,g or less of pseudoephedrine pe r recorr,tr.ended dosage unit ~ or
(b) 10 liquid prepai'alions containing 60rr,g or less of pseudoephedrine per recoff,mended adult dose.
PYRANTEL for hurr,an therapeut lc use.
PYRITHIONE ZINC for hurr,an therapeutic use, <:.,:,c:::e~ in preparations containing 2 per" cent or less of pyrithione zinc, when:
Ca) in serr,isolid halr preparaclOns, or
(b) in shaff,poos.
SALICYLAMIDE <;,,:,~,,,e,=:
(a) when included in Schedule 3,
(b) ln indiVidually wrapped powders or sachets of granules each containing 1 000 rr,illigrams or less of salicylamide as the only therapeutlcally active consLituent when:
(i) the pack is labelled with the warning statement:
... /11.
1
)
)
)
I,
)---
)
"
(Ii 1
- 11 -
WARNING - nas ~JEDl.CATlON bAY BE DANGEROUS \~HEN USED IN LARGE ANOUNTS OR FOR A LONG PE:RlOD, or
CAUTION - nns PREPARATION IS FOR THE RELIEF OJ' HINOR AND TEHPOl1.ARY Al Ll'JE.NTS AND SHOULD BE USED STRI CTLY AS DI[{ECTED. PROLONGED USE WITHOUT [,.EDlCAL SUPERVISlON COULD BE llARHFUL" and
in a prlnlary pack containing not. more than 12 such powders or sacheLs of granules; or
(c) tablees or capsules each containIng 500 milligrarr,s or less of salicylarr,ide as the only therapeutically active constituent when;
(i i)
(iii)
the pack is labelled with the warning staterr.ent;
vJARNING - TllI3 l"lEDICATlON HAY BE DANGEROUS WHEN USED IN LARGE AHOUNTS OR FOR A LONG PEIUOD, 0 r
CAUTION - THIS PREPARATION IS FOR THE RELIE~- OF [,INOR AND TE~IPORARY AILHENTS ANlJ SHOULD BE USED STRICTLY AS DIRECTED. PIWLONGEP USE WITHOUT HED1CAL SUPERVISION COULD BE HARMFUL, and
packed in bl ister or strip paCkaging or in containers with a Child-resistant closure, and
1n a pri.l'Lary pack conLainLng nQe rr.ore than 25 such tablets or capsules.
SILVER SALTS for th"rapeuttc use, E!~~ept
(a) chehing LableLs containing 5cr,g or less of silver per tablet, or
(b) solutions containing 0.3 per cent or less of silver.
SODIUM NITRITE for therapeutic use,
SPUTOLYSJN - See t cans - 4- «(3, 5-dibrorr,0- 2- hydrOl<ybenzyl) -acr,i no) cyclohexanol hydrochloride rr,onohydrate ..
STAPHISAGRIA e.",:,~\?,t. in preparaLions concalning 0.2 per cent or less of staphisagria.
STRAMONIUM in preparations conLdlnlng 0.25 per cent or less of the alkaloids calcurated as hyoscyamine, e..~~E!!?.~ preparations for smoking or burning.
TETRAHYDROZOLINE
THENYLDIAMINE
Cal in nasal preparalions for topical use, or
(b) when compounde.d with one or more of t.he following rr,edicarr,ents,
(i) an anLilusslw e~~ee~ codeine or dihydrocodelne"
(ii ) an expeClorant, or
( HI)
•.. /12,
- 12 -
except in preparatiotls for the treatment of children under 2 yea'rso f age.
TRAMAZOLINE
TRIMEPRAZINE when corr,pounded WiLh one or IT,ore of the following medicarr,enrs.
(a) an antitussive ",-"c:e,e,~ codeine or dihydrocodeinei
(b) an expectol'ant or
<:"c:~p~ in preparations for the treatrr,ent of children under 2 years of age.
TRIPROLIDINE when corr,pounded with one or more pf the following medicarr,ents'
TYMAZOLINE
(a) an antitusslVe "-,,c:~e.~ codeine or dihydrocodeine.
(b) an expectorant, or
",-"<:,,,-p~ in preparations for the treatment of children under 2 years of age,
XYLOMETAZOLINE
I'e, I
)
)
)
)
)
SCHEDULE 2
ACEPIFYLLINE in liquid oral preraral: ions.
ADRENALINE 1n preparallons conta1ning 1 per cent or less of adrenaline ~<;:<:J'~ In preparations containing 0.02 per cenL or less of adrenaline.
AMINOPHYLLINE in liquId oral preparaLlons.
AMYL NITRITE
BENZOYL PEROXIDE: in preparati.ons conLainwg 10 per cent or less of benzoyl peroxide for external hun,an therapeutic use" <:If'::,<:ec when included in Schedule 1.
BROMPHENlRAMINE in oral preparatlons <:?'~<:e~ when included in Schedule 1.
BUCLIZINE in oral preparaLions ">':':<:P.~ when included in SChedule 1.
FUTY!. NITRITE
C;,LORAL HYDRATE fo r bun,an ince r nal therapeut ic use in preparat ions conLa Lning 5 ,·cr cent or less of chloral hydrate, when packed in containers of 100 IT,l or It:~ss~
CHLOROFLUOROCARBONS - see FLUOROCARBONS
CRLORPHENlRAl!1INE in oral preparaLions e",<;:ept; when included in Schedule 1.
CLEMASTINE in oral preparaLions.
CLOTRlMAZOLE" for hun,an use in preparatlOns COntaln1ng 1 per cent or less of clotri.n,azole, for treatn,ent of fungal infections of the skin.
CODEINE 1 n tablets or capsules each cOntaining 10".g or less of code lne when con,pounded witb asp1nn. paracetamol or salicylamide or anyone of Lheir derivat.ives and no other 4nalgeslc substance) ~.~c:~e~ tllhen included .in Schedule 1.
CYPROHEPTADINE in oral preparat ions.
DEXCHLORPHENIRMHNE in oral preparaLions E!'!.":~f'~ when included in Sc~edule L
D1HYDROCODEINE, when con,pounded with one or n.Ore otber therapeutically aCLive substances wh.en;
(a) in divided preparations Containing 10 mg or less per dosage unit and ,'ith a recommended dose nOt exceeding 1Smg of dihydrocodei.ne; or
(b) In undivided preparations containing 0.25 per cent or less of dihydrocodeine with a recorr,rr.ended dose not exceeding i5mg of d ihydrocode ine.
. .. /2.
, "
- 2 -
DIHENHYDRINATE in oral preparalions "',~~C:P': when included in Schedule 1.
DIHETHIND]1;NE in oral preparaLi.ons.
DIPH]1;NHYDRAMtINE in oral preparations e.~~"2t: when included J.n Schedule 1.
DIPHENYLPYRALINE in oral preparaLions ~'.:~"e.t: when included in Schedule 1.
DITHRANOL for human therapeutic use.
DOXYLAMINE in oral prepa"a;: ions ",~~~p,~ when included in Schedule 1.
ECONAZOLE for hurr.an use in preparar. ions conlaining 1 per cem or less of econazole for treatment of fungal infections of the skin.
EPHEDRINE for internal use when corr-pour,ded with one ally active substances, other than preparations supression or weight controlj;~r-po-se·s~·~ ~~~~p.E-::
(a) when included in Schedule 1. or
or rrlore other therapeuticfor stimulant, appetite
(b) i.n liqUid prepar-al ions comaining 10rr.g or less of ephedrine per recoIT.mended dose.
FENOTEROL in rr.etered aerosols delivering 200 microgra",s or less of fenoterol per metered dose.
FLAVOXATE
FLUOROCARBONS and CHLOROFLUOROCARBONS alone or in corr.bination wlth other propelants or refr igarant.s in liqui Hed gas forq. for therapeutic use.
FOLIC ACID for hU!,.an therapeutic use except in preparations containing 500 ".lcrograms or less of folic acid per reco;;.rr.e~·ded da ily dose.
FOLINIC ACID for hurr.an therapeutic use ".~~e.!"t: in preparations comaining 500 rr.icrograrr.s or less of folinic acid per recorr.mended dady dose.
FOLINIC ACID for human ther-apeutic use except in preparations containing 500 rr';,crograrr.s or less of fol inic acid per rec(;ffi;r:e'nded daily dose.
HYDROCORTISONE and HYDROCORTISONE ACETATE as the only therapeutically accive s'iibstancesln'preparat'lons'ror demal use containing 0.5 re.r cent or less of hydrocortisone in packs conl.alning 30 grams or less wi.1ere the labelling warnS against contact with the eyes and against use for acne and on children below 2 years of age. lise beyond 7 days, and use under occlusive dressings. except on IT!edtcal advice.
IDOXURIDINE in preparations containing 0.5 per cent or less of idoxuridi.ne for cuLaneous use .
. INSULIN
ISOCONAZOLE for burr.an use in preparat ions cOntaining 1 per cent or less of i,oconazole. for treatment of fungal infections of the ski.n.
.. ./3
)
)
)
)
)
)
- 3 -
LOPERA~l1DE in packs of " dosage unLl.s or less, each dosage unit concaining 2rr.g or less of loperarr,ide.
MEFENAMIC ACID Ln racks of 30 0, less capsules for treatIT.ent of spas<l.odi.e dys!Jlenorrhoea.
MEPYRAMINE in oral prepaeaL ions.
HETHDILAZINE 1n oral preparauoos.
HICONAZOLE for hurr.ao use .In j>ceparat 1005 eoocaioing 2 per cent 01.' les of rr.iconazole for treatrr.ent of fungal infections of the skin.
NAPROXEN in packs of 12 or less tablets for capsules. for treatmenL of spasIT,odic dys%enorrhoea"
NITROPFURAZONE in preparat lOll for cutaneous use containing 0.2 per eenc or less of nit roful~azone.
OeTYL NITRITE
PHENlRAMINE in oral preparaeins e.~c::ep'~ when included in Schedule 1.
PHENYLPROPANOLAMINE in preparat ions for rellef of coughs or colds. containing 25 "'g or less per dose of phenylpropanoiarr,ine.
PHENYLTOLOXAMIINE in oral preparations.
PODOPHYl.LUM RESIN (Podophy 11 in) containing 20 per cent or leGS of 1.
for external bUffian use in preparations podophyll in e.!!.":",.et "hen included in Schedule
PROl'iETHAZINE in oral preparations ex<:-e.p~ when included in Schedule 1.
PSEUDOEPHEDRINE "~,,:,,p~ when included in Schedule 1 or 3.
QUININE for hurr,an internal therapeutic use except in liqUids containing 4O:t,g/L O~ less of quinine.
SALBUTAMOL
SANTONIN
(a) in rr,elered aerosols del i.vecJ.ng 100 rr,icrograrr,s or less of salbutaulol per !j,etered dose. or
(b) in capsules of dry powder for inhalation delivering 200 ITlicrograms or less of salbut.amol pe,," dose.
SODIUl'I CROMOGLYCATE in nasal preparations for topical use.
TERBUTALINE in met.ered aerosols delivering 250 m;crograrr,s or less of terl:lUtaline per metered dose.
.. ./4
, ,
- 4 -
THENYI..DIAHINE in oral preparac ions "x<::~eE. when included in Schedule 1.
rmWPHYl..l..INE in liquid ol'al preparat.lons,
lIOCONAZOLE for human use in prparauons containing 1 per cent O[ less of ioconazole" for treatment of fungal infections of the skin.
TRETINOIN for external human therapeutic use.
T RIMEPRAZINE
(a) ln solid oral preparallons, or
(b) in llqUld oral prepacations containing 10mg or less of trlmeprazine per 5ffil~
~~c:.",p.~. when included in Schedule 1.
TRIPROLIDINE in oral preparat ions "'l<C:"P~. when included in Schedudle 1.
•
"
SCHEDULE 3
(Substances marked + are listed in the NOlice)
ACEBUTOLOL
ACEPIFYLLINE !'.~,,"e."e!' when included in Schedule 2.
ACEPROMk\\ZINE
~) ACETANILIDE and alkyl aceLanilldes, for human therapeutic use.
ACETAZOLAMIDE
ACETOHEXAMIDE
") ACETYLCHOLINE and other choll ns eSLer 5 <a.~<:"'.2t" when separacely specified in this Schedu Ie.
)
r--
)
J
ACETYLCYSTEINE
ACETYLDIHYDROCOJ)EINE, when corr.pounded With one or more other medicarr.entso
(a) in divided preparaLions cOntalning not more than lOOmg of acetyldihydrocodeine pe r dosage unit, or
(b) in undivlded preparallons .,ilh a concentratlon of not more chan 2" 5 per cent of ace tyldlhydrocodeine.
ACETYLMETHYLDIMETHYLOXIMIDOPHENYLHYDRAZINE
ACYCLOVIR
ADlPHENINE
ADRENALINE ,,}{<:~J)~ "
(a) when included in Schedule 2; or
(b) in preparal.ions conLaining 0.02 per cent or less of adrenaline.
ALCURONlUM
alpha .. CHLORALOSE .. See chloe-alose
ALPHADOLONE
ALPHAXALONE
ALPRAZOLAM
ALPRENOLOL
ALPROSTADIL
AMANTADINE
AMBENONIUM
AMBUCETAlHDE
ABBUTONIUM
... /2.
- 2 -
AMETHOCAINE
AlllKACIN
AHlLORlDE
AHINOCAPROIC ACID
AHINOGLUTETHIMIDF.
AMINOMETRADINE
AMINOPHENAZONE and derivatives therefrom for the treatrr,ents of anLrr,als.
AMINOPHYLLINE ".:><~~e~ when included in Schedule 2.
AHINOPTERIN
MIINOREX
AMlODARONE
AMIPHENAZOLE
Ai'lISO~1ETRADlNE
MIITRIPTYLINE and ot:her corr,pounds structurally deoved therefro(f, by substitution In the side chain ":><c,,e~ when separately specified in this Schedule.
Ml0DIAQtJINE
Al'10XYCILLIN
Ai!lPHO~jYCIN
AMPHOTERICIN
Al"IPICILLIN
AMSACRINE
AMYLOBARBITONE when packed and labelled for injecLlon.
AMYLOCAINE
ANABOLIC STEROIDAL AGENTS ~x~ee:: when separately specifIed in this Schedule.
ANGIOTENSINAMIDE
ANTAZOLINE "XC:O:l'.l. when lncluded in Schedule 1.
+ANTlBlOTlCS exc:"j~~'
, .. /3.
, I
)
1
1
)
,--- -
)
.. 3 -
(a) when SC0ara[cly specifled In these Schedules~
(b) avOparcin when ,Jacked and labelled for use as an anirr,al feed addiLive J or
(c) n1.Sin.
ANTIHISTAMINES
(a) when included in Schedule 1 or 2., or
(b) when sapa,atcly specified in thIs SChedule.
ANTUJALARIAL SUBSTANCES <::<~eet when separaLely specified in this Schedule,
ANTU10NY .. ol'gao.'c coo,pounds of, for therapeuLic lise.
ANTITUBERCULAR SUBSTANCES i.ncluding ar{,i Ilosal icyc l ic aC1(l and thiacetazone Schedules.
lsonlazid and its dertvaLives, para· e~~!e~ when separately specified in these
APOMORPHINE
APROTlNIN
ARSENIC see THIACETARSAMlDE
ASPIRIN \<hen combl ned wi Lh caffe lOe . ;J ... acetarr,ol or saitcylarr.l de 0 r any Jel'ivative of these substances.
ATENOLOL
ATROPINE HETHONlTRATE
AURANOFlN
AZAPERONE
AZAPETlNE
AZATADINE
AZLOCILJ..IN
AZTREONAi1
BACAMPICILLIN
BACITRACIN ex~~et:
BACLOFEN
BAMIPINE
(a) when s~eclfied In the Notice
(b) in aOlIT,al feeds for growth prorr,ollon containing 5Or.g/kg at' less of antibiotic substances, or
(c) in rr.iH{ replacers for calves and starter rations for pigs, contaIning IOOmg/kg Ot less of antibiotic substances.
.. ,/4,
- 4 -
BARBITURIC ACID and Jto de",~vati.ves ex,,:e,pt,'
(a) "hen included or separately specified in the Notice, or
(b) "hen separately specif,ed in th.s Schedule,
BECLAI1ID£
BE1'lEGRWE
BENACTYZINE and ottler substances structurally derived froIT. diphenylmethane "i th ataractic properties ~vhen used for therapeutic purposes.
BENDROFLUAZIDE
BENORYLATE
BENS£RAZIDE
B ENZAl1INE, <:"",<:P-t.', "hen inc I ude d in Sched ule 1.
3ENZHEXOL
,'>llNZlLONIUM
;)ENZOCAINE, ~,,,c:<:i~,~ when included in SChedule 1.
LIcNZODIAZEPINE denvatives "xc:ept \Vhen se"arately specified in these Schedules.
l)ENZOYJ. PEROXIDIl1 in preparations for e"ternal hurr,an therapeutic use, ""C:E!ei:. when included in Schedule 1 or 2.
BENZPHETAMINE and oLher substances st ructurally de t' i ved from beta-arr.! nopropylc.enzene or beta-arr,inoisopropylbenzene by substitution in the side-chain or by 'Lng-closure tr.ercin (or by both sucr. subst.1[ution and such closure) <)x<:E!e~'
Ca) where se,Jaraldy specified in this or any other Schedule; or
(b) ephedrine and pseudoephedrine in preparacLons exempced ft"oITI Schedule L
BENZTROPINE
----- BENZYHAJilIINE ~~~~e~_ wbeo included in SChedule 1,
BENZYLPENICILLIN (including procalne penlcillin) "J{c:~e,t, when specifled in the Notice.
BETAHISTINE
BETHANlDIN£
j) IFONAZOLE
, .. /5,
)
)
)
"
- 5 "
BIPERlDEN
BISl'1UTH corr,pollnds of, for burr,an therapeutic or Costr,eeic use, ~~c::~Pt:
llLEOHYCIN
(a) bisrr,uth CIleace when incorporated in haIr colour ant preparations in concentracions of 0.5 per cent or less~
(b) bismuth oxychloride in cosff,etics, or
(c) bisa,ulh fomic iodide or bismuth subiodide in dusting powders Containing 3 per cent or less of bismuth.
BORON for hurr,an therapeutic use"
Bi{ETYLIUH
BROMAZEPAM
(a) for internal use
(b) in glycerines or honeys of borax or boric aCid.
(c) in dusLlng powders for paediaLric use; or
(d) as a tr.erapeut tcally aCllve ingredient: 1n oLher preparaUons for de m,a I us e ~!.'C::,"P."t,
(1) In antifungal preparations, Or
(li) in preparatl.Ons containing 0.1 per cent or less of boron.
Bl10MIDES~ inol'ganie" for. therapeutic use.
BROHOCRIPTlNE
BROHOFORM for therapeutic use.
BRONPHENIRAII1INE ".x~epE when included in Schedule 1 Ol" 2,
BROHVALETONE
r----- BUCLIZINE ~"C:;':P.~ when inclUded in Schedule 1 or 2.
)
)
BUFRXAMAC except in prepa, aClons can, alning 5 per cenl or less of bufexarr,ac for external hUrf,an -therapeutic use ~ including suppositori.es.
BUHETANlDR
BUPIVACAINE
+BUPRRNORPHINE
BUSPIRONE
... /6.
BUSULPHAN
llUTACAINE
- 6 -
DUTYLAlllNOBENZOATE ,:'.'c:epL when included i.n Schedule 1.
BUTYLCHLORAL HYDRATE
CALCITONIN
CALCITRIOL
CALCIUM CARBIHIDE for therapeuuc use.
CAMPHORATED OIL excludlng admixtures.
CAMPHOTMIIDE
CANDICIDIN
CANINE TICK ANTI-SERUM
CANTHARIDIN
CAPREOMYCIN
CAP'fODlABE
CAPTOPRIL
CAPURlDE
CARAMIPHEN
CARBACHOL
CARBAHAZEPINE
CARBARYL for hurr,an therapeutic use e'.'<:<:l'.1: when incluc1ed in Schedule 1.
CARBAZOCHROHE
CARBENICILLIN
CARBENOXOLONE e~'O.~.l'.~ when included tn Schedule 1-
CARBIDOPA
CARBlHAZOLE
CARBOCROMEN
CARBOPLATIN
CARBROHAL
... /7.
)
)
)----
)
)
)
- 7 -
CARDIAC GLYCOSIDES <:~~~~Pt. "hen separately specifIed in these Schedules.
CARINDACILLIN
CARMUSTINE
+CARNIDAZOLE
CEFACLOR
CEFOPERAZONE
CEFOTAXIME
CEFOTETAN
CEFOXITIN
CEFTAZIDIME
CEFTRIAXONE
CEPHACETRILE
CEPHADROXIL, for the trea!: mem of anmals.
CEPHALEXIN
CEPHALORIDINE
CEPHALOTHIN
CEPHAl1ANDOLE
CEPHAPIRIN
CEPHAZOLIN
CEPHRADINE
CHENODEOXYCHOLIC ACID
CHLORAL FO~IDE
CHLORAL HYDRATE ~x~.,,!'..~:
(a) "hen included in Schedule 2, or
(b) in preparations for tOi"cal use conLaining 2 per cent or less of chloral hydrate.
CHLORALOSE ""c:"p~ when sf)ec If led in t he No t ice.
+CHLORAMPHENICOL
CHLORAZANIL
••• / iJ •
- (j -
CHLORBUTOL in preparations for human oral use, except in preparations containing 0,5 pc r cent or less of chlorbutol as a preservaiive:-
CHLORCYCLIZINE
CHLORDIAZEPOXIDE
CHLORMERODRIN
CHLORMETHIAZOLE
CHLORMEZANONE
CE.LOROFORi'l for' use in anaeSthesia.
?- (4.CHLOROPHENYL) .. 1,2, 4-TRIAZOLE [5, la] - ISOQUINOLINE for the treatment of ')li:'T,als.
CHLOROQUINE
GHLOROTHIAZlDE
CELORPHENIRAMINE ~J<:~<:E'!' '''hen included in Schedule 1 or 2.
C,ILORPIlENTERMINE
VtLOL{PROPAMlDE
S,)LORTETRACYCLINE ".1{<:;<:et when spec if J cd In the No t ice
CHLORTHALIDONE
~:'iLORZOXAZONE
',;HOLESTYRAHINE for human thcrapeuClC use,
CHYMOPAPAIN; injecl.ion foe hurr,an therapeut ic use.
CICLACILLIN
CILASTAT1N
CIMETIDINE
CINCHOCAINE
CINOXACIN
CISPLATIN
CLANOBUTIN. in injec'-1ons for the treatment of aniu;als.
CLAVIILANIC ACID
CLEMASTINE "xc:~p~ when included in Schedule 2.
. .. /9
,
"
)
)
,
)
)
)
- 9 -
CLEMIZOLE
+ CLENBUTEROL
CLIIlINIUM
CLINDAMYCIN
CLOBAZAl1J
CLOBETASONE-17-BUTYRATE
CLOFENAl'IIDE
CLOFIBRATE
+CLOMIPHENE
CLOMIPRAl'IINE
CLOMOCYCLINE
CLONAZEPAM
CLONIDINE
CLOPAl'1I1lE
+CLOPROSTENOL
CLORAZEPATE
CLOREXOLONE
CLORPRENALINE
CLOTRIl1AZOLE, <:~<::"e_~ when included i.n Schedule 2 or in the Notice.
CLOXACILLIN
CLOZAPINE
CODEINE, except when included in Schedule 1 or 2, when corr,pounded with one or ",ore other-t:h,ir--:'peutically active substances:
(a) in divided preparations cOntainlng 30mg or less of codeine per dosage unH, or
(b) in undivlded preparaLions containing 1 per cent or less of codeine.
. .. /10.
- 10 -
COLASPASE
COLCHICINE
COLESTIPOL for human therapeutic usa·
COLISlIN
CORTISONE and "ceroid suprarenal cort lcal horITooncs, e.!<~':'I?.t hydrocortisone in Schedule 2.
CURARE, TUBOCURARINE, d-TUBOCURARINE, d··TUBOCURARINEIllIMETHYLETHER and all synthetic quaternary arr.monim. corr.pounds and other corr.pounds having curarislng properties <:~,,~£~ when separately specified in t. hi s Schedule.
CYCLANDELATE
CYCLIZINE
+CYCLOFENIL
CYCLOPENTOLATE
CYCLOPROPANE for therapeutic use .
. CYCLOSERINE
CYCLOSPORIN
CYCRIMINE
CYPROilEPTADINE ,:,,,,,,e.!'~. "hen included in SChedule 2
DACARBAZINE
DANAZOL
DANTROLENE
DAPSONE and all deCivatives of 4,4-dian.inodlphenylsulphone.
,DEANOL
DEBRISOQUINE
DEMECARIUM BROMIDE
DEMECLOCYCLINE
DESIPRAMINE
DESMOPRESSIN (D.D.A.V.P.)
+DETOMIDINE
... /11.
"
)
) . ,
')
)
)
y--
)
)
- 11 -
DEXCHLORPHENIRAMilNE <:~C:<:f't when included in Schedule 1 or 2.
DEXTRONETHORPHAN~.:<:c.<:pt when included in Schedule 1.
+DEXTROPROPOXYPHENE
(a) in divIded preparations cOntainH'g 135~.g of dextropropoxyphene or less per dosage unit .. or
(b) liqUid preparations containing 2.5 per cent or less of dextropropoxyphene.
DEXTRORPHAN
DIAZEPAM
DIBENZEPIN
TRANS-4-«3,5-DIBROMO-2-HYDROXYBENZYL)-AMINO) CYCLOHEXANOL HYDROCHLORIDE MONOHYDRATE (Sputolysin) <:~c:<:p~ when in Schedule 1.
DICHLORALPHENAZONE
DICHLORPHENAMIDE
DICLOFENAC
DICYCLOMINE "~C:~F.'t when included in SChedule 1.
DIETHAZINE
DIETHYLCARBAMAZINE fa r hu~.an t herapeut ie use.
DIETHYLPROPION
DIFENOXIN in preparaLions containing, per dosage unit, O.5mg or less of difenoxin and a quantity of atropine sulphate equivalent to at least 5 per cent of the dose of difenoxin ..
DIFLUNISAL
DIGITALIS and its glycosides.
DIHYDRALAZINE
DIHYDROCODEINE when compounded with one or more other rr.edicaments:
(a) in dlvlded preparatLOns containing not u.ore than 100mg of dihydrocodeine per dosage unit. or
(b) in undivided preparations with a concenLration of noc more than 2.5 per cent of dihydrocodeine.
~J<:C:"P[ when included in Schedule 1.
... /12.
'-J'
. 12 . ' .
DIHYDROSTREPTOMYCIN e.,:~"er: when spec If ted in ehe Not ice.
DIISOPROPYLAMINE DICHLOROACETATE
DILTIAZEM
DIMENHYDRINATE e."C::.~P'£ when included in SChedule 1 or 2.
DIMETHINDENE ~~~~p.~ when included in Schedule 2.
DIMETHISOQUIN ~~C::~P.t; when included in Schedule 1.
DIMETHOXANATE
DIMETHYL SULPHOXIDE for therapeutic use ,,-xc::~p~ when specified in the Notice.
DINITROCRESOLS for therapeutic use.
DINlTRONAPHTHOLS for therapeutic use.
DINITROPHENOLS for therapeutic use.
DINITROTHYMOLS for therapeutic use.
+DINOPROST
DIPERODON
DIPHEMANIL METHYLSULPHATE ~~c::e.p~ when included In Schedule 1.
DIPHENHYDRAMINE "."c.",pt when wcluded LO Schedule 1 or 2.
DIPHENIDOL
DIPHENOXYLATE in preparations contaIning per dosage unit 2.5mg or less of dlphenoxylate and a quantity of atropine sulphate equivalent to at least 1 per cent of the dose of diphenoxylace.
DIPHENYLPYRALINE e.,,~e.e~ when included in Schedule 1 or 2.
DIPIVEFRIN
DIPYRIDAMOLE
DISOPHENOL
DISPYRAMIDE
DISULFIRAM for therapeutic use.
DlTHIAZANINE e.~~ee~ when specified in the Notice.
DOBUTAMINE
DOMPERIDONE
DOPAMINE
DOTHIEPIN
)
)
, ,
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) -
)
)
"
- 13 -
DOXAPRAM
DOXEPIN
DOXORUBICIN
DOXYCYCLINE
DOXYLAMINE "!'~~Et. when included in SChedule 1 or 2.
DROPERIDOL
DROSTANOLONE
ECONAZOLE !'2':~"p.,!: when included in Schedule 2 or in the Notice.
EDETIC ACID for hUll,an therapeutic use in preparations for injection or infusion.
EMETINE ~>:~"p.~, in preparations cO,ntaining 0.2 ,per ,cent or less of emetine.
ENALAPRIL ,
EPHEDRINE ~!'~~et.;
(8) when included in Schedule 1 or 2,
(b) in preparations for topical use containing 1 per cent or less of ephedrine, or
(c) when compounded with one or (I,ore other therapeutically active substances in 1 iquid preparations for internal use containing 10mg or less of ephedrine per recoll,q,ended dose, other than prepa rat ions for st i mulant. appet ite suppress ion ·ci;'-·-:W" igtlt control purposes.
ENFLURANE for therapeutic use.
EPICILLIN
EPIRUBICIN
ERGOT
ERYTHROMYCIN ~~c.~~~:
(a) when specified in the Notice,
(b) in an1mal feeds for growth proll,otion containing 5Orr.g/kg or less of antibiotic substances; or
(c) in milk replacers for calves or starter rations for pigs, containing lOOmg/kg or less of antibiotic substances •.
ETHACRYNIC ACID
ETHAMBUTOL
... /14.
- 14 -
ETHAMIVAN
ETHCHLORVYNOL
ETHER for use in anaesLhesla.
ETHINAMATE
ETHOGLUCID
ETHOHEPTAZINE ~?':.c.~J'~,1O when included in Schedule 1.
ETHOPROPAZINE
ETHOXZOLAMIDE
ETHYL CHLORIDE for inhalation anaesthesia.
ETHYLMORPHINE when compounded wier. one or more other tT.edicaments;
(a) in divided pre~arations containlng not more 'than 100mg of ethylmorphine per dosage unit, or
(b) in undivided preparations wilh a concentration of not rr.ore than 2.5 per cent of ethylmorphine;
':?':<:.':P!: when included in Schedule 1.
ETHYLOESTRENOL
ETlDOCAINE
. ETIDRONATE ~~<:':!'''. in tooth pastes and gels COntaining 1 pe r cent or less of etidronate.
ETILEFRIN HYDROCHLORIDE
ETOPOSIDE
+ETRETlNATE
FELYPRESSIN
FENCAMFAMIN
FENFLURAHINE
FENOPROFEN
FENOTEROL ~?':.C:~.p.~ when included in Schedule 2.
FENPIPRAMlDE
FENPIPRANE
+FENPROSTALENE
... /15.
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- 15 -
FLAVOPHOSPHOLIPOL ~~<:~!'t:
(a) Vlhen specified 1n the Nolice, or
(b) 1n animal feeds for growth pronotion containing SQrr,g/kg or less of antioiotic substances.
FLECAINIDE
FLUCLOXACILLIN
FLUCYTOSINE
FLUFENAMIC ACID
FLUNISOLIDE
FLUNlTRAZEPAM
FLUNIXIN MEGLUMINE for the treatment of animals.
FLUORIDES in preparalions for human ingebllon e.~<::e.!.',:: when included in SChedule 1.
FLUOROURACIL and other substances structurally derived frorr, uracil Vlith cytotoxic properties Vlhen used for therapeutic purposes.
FLUOXYMESTERONE
FLUPHENAZINE
+FLUPROSTENOL
FLURAZEPAM
FLUROXENE for inhalation anaesthesia
FLUSPIRILENE
'+FOLLICLE STIMULATING HORMONE (See also gonadotrophins)
FRAMYCETlN
FRUSEMIDE
FUSIDlC ACID
GALANTHAMINE
GALLAMINE
GEMEPROST
GENTAMCIN
... /16.
- 16 -
GLlBENCLAMIDE
GLIBORNURIDE
GLICLAZIDE
GLUCAGON
+GLUTETHIMIDE
GLYCERYL TRINITRATE in preparations for injection.
GLY~OPYRROLATE
GLYMIDINE
GONADORELIN
GONADOTROPHINS ~~~~p.~ when inc luded in Schedule 1.
GRAMICIDIN
GRISEOFULVIN
GROWTH HORMONE
GUAIPHENESIN ,,:<<::~p.t. when included in Schedule 1.
GUANABENZ
GUANACLINE
GUANETHIDINE
HALCINONIDE
I
'.
HALOPERIDOL and other substances structurally dertlTed frau. butyrophenone with ata ract ic prope rt ies when used for the rapeutlc purposes. except when separatel y specified 1n this Schedule.
KAl,.OTHANE for therapeut icuse.
HEPARIN for internal therapeutic use.
HETACILLIN
HEXACHLOROPHANE
(a) in preparations for use on infants, or
(b) in other preparations ~,,~,ee~ when included in Schedule 1 or specified in the Notice.
.. ./17.
, .
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• 17 .
HEXAMETHONIUM
HEXOCYCLIUM
HYALURONIC ACID in preparations for injection.
HYDRALAZINE
HYDROFLUMETHIAZIDE
HYDROQUINONE for hUIT,an therapeuttc use ~.':'<:"I'E. in preparations containin8 2 per cent or less of hydroquinone.
HYDROXY CHLOROQUINE
I-HYDROXYPYRIDO (3.2,a)-5·PHENOXAZONE-3-CARBOXYLIC ACID
HYDROXYUREA
HYDROXYZINE
HYGROMYCIN ,,~S~E~;
(a) when specified in the Notice, or
(b) in preparations in concentrations of SOmg/kg or less of antibiotic subscances.
HYOSCINE BUTYLBROMIDE
HYPOTHALAMIC RELEASING FACTORS ~~S"l'~ when separately specified in this Schedule.
I BUFENAC
IBUPROFEN
IDOXURIDlNE ,,~<:e.p'~. when included in Schedule 2.
IMIPENEH
IMIPRAMINE
INDAPAHlDE
INDOMETHACIN
INOSITOL NICOTINATE, for internal use.
ION·EXCHANGE RESINS, anionic and cationiC, for interal use in humans "':'S"p.£ when separately specified in this Schedule.
IOPAHlDOL
" ./18.
, . - 1 il -
I PRATROPIUN
IRON compounds in injectable pre;>arat:ions for hurr,an therapeutic use.
ISOAMINILE
ISOCONAZOLE ~::~~f.'.,t when included in Schedule 2 or specified in the Notice.
ISOETHARINE
ISOFLURANE
ISOMETHEPTENE
ISOPRENALINE
ISOPROPAMIDE ~~~e.e~ when included in SChedule 1.
+ ISOTRETlNOlN
ISOXUPRINE
KANAMYCIN
KETAMINE
KETOCONAZOLE
KETOPROFEN KHELLIN,
K I TASAMYCIN ~::~~,r.,t.:
(a) when specified In the NOtLce. or
(b) in anirr,s feeds for growth pro(f,oLion containing lOQrr,g/kg or less of antibiotic substances.
LABETALOL
LATAMOXEF
LAUDEXIUMMETHyr;SULPHATE
LEAD COMPOUNDS for human therapeutic use.
LEFETAMINE
LEP',rAZOL
LEUPRORELIN
LEVALLORPHAN
... /19.
I "1
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)
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- 19 -
LEVAMISOLE
(a) for human therapeutic use. or
(t) in preparations for the prevention or trea[~eni of heartworm in dogs.
LEVODOPA
L IDOFLAZINE
LIGNOCAINE ~~c~e~ when included in Schedule 1.
LINCOMYCIN
LINDANE for hurr,an therapeutic use e,,~.~e.~. when included· in Schedule t.
LIOTHYRONINE SODIUM (Triiodothyronine).
LITHIUM salts for therapeutic use, ~.x~e.!)E:. in preparations containing 0.01 per cent or less of litnium.
LOPERAMIDE ~,,~~I~~ when included in Schedule 2.
LORAZEPAM
LOXAPINE
+LUTEINISING HORMONE (See also gonadotrophins).
LYMECYCLINE
MAFENIDE
MALDISON for hurr,an therapeut ic use ~l{~".e~ when included in Schedule 1.
MAPROTlLINE 'I: ".
MAZINDOL
MEBEVERINE
- MEBHYDROLIN
MECAMYLAMINE
MECLOFENOXATE
MECLOZINE
MEDAZEPAM
MEFENAMIC ACrD ".~~~p~ when incuded in SChedule 2.
MEFLOQUlNE
... /20,
- 20 - ,
MEFRUSlDE
MEPACRINE
MEPENZOLATE
MEPHENESIN and its denvatives e.~£,:,e.~ guaiphenesin where specified in Schedule 1 or 3.
MEPHENTERMINE
MEPIVACAINE
MEPROBAMATE
MEPYRAMINE ':'}{c;eeE when included in Schedule 2.
MERCAPTOPURINE and other substances structurally derived therefrom with cytotoxic properties when used for therapeutic purposes.
MERCUROUS CHLORIDE for internal therapeutic use.
MERCURY ORGANIC COMPOUNDS for therapeutic use, ~,,£e.e~ when included in Schedule 1.
METARAMINOL
METFORMIN
METHACYCLINE
METHANDIENONE
METHANDRIOL
METHANTHELINIUM
METHAZOLAMIDE
METHDILAZINE ,:,~£e.e~ when included in Schedule 2.
METHENOLONE
.... METHICILLIN
METHIMAZOLE
METHIXENE
METHOCARBAMOL
METHOTREXATE
METHOXSALEN
METHOXYFLURANE for therapeutic use.
METHYLANDROSTANOLONE
.• • /21.
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, - 21 -
METHYCLOTHIAZIDE
METHYLDOPA
METHYLPENTYNOL and other substituted alkynes for internal use.
METHYPRYLONE
METOCLOPRAMlDE
METOLAZONE
METOPROLOL
METRIZAMlDE
METRONIDAZOLE including benzoylrr.etronidazole
METYRAPONE
MEXILETlNE
MEZLOCILLIN
MIANSERIN
MIBOLERONE
MICONAZOLE, "~<:,,e£ when included in Schedule 2 or in the Notice.
MlDAZOLAM
MINOCYCLINE
MINOXlDIL
MlS0PROSTOL
MlTHRAMYCIN
MITOBRONITOL
MITOMYCIN
MITOZANTRONE
MONENSIN ~~£~e~;
(a) when specified in the Notice. or
(b) in animal feeds containing 33mg/kg or less of antibiotic substances ..
MONOAMINE OXIDASE INHIBITORS, including iproniazid, isocarboxazid, nialarr,ide, phene lzine. pheni prazine and other preparations for which rr.onoan,ine oxidase i nhibiL ion is claimed, ~,~~~.e~ triparanol.
. . . /22.
• 22 .
MONOBENZONE for hurr,an therapeutIc use <:",~<:e~ in preparations containing 2 per cent or less of ffionobenzone.
MOPERONE
MUPIROCIN
MUSTINE and other subsr.ances structurally derived Lherefrom· with cytotoxic properties, when used for therapeutic purposes ",?'"",!,~ when specified in this Schedule.
NADOLOL
+NALBUPHINE
NALIDIXIC ACID,:,?'£,:,l'!: when spe,cified in the NoUce,
NALORPHINE
NALOXONE
NANDROLONE
NAPROXEN ':?'<:':'f'.t. when included in Schedule 2.
NARASIN .':'?'~."f'~.:
(a) when specUied inth" NoUce. or
(b) in ani",al feeds containing lOOn,g/ltg or less of narasin.
NATAMYCIN
NEOMYCIN ",,,£e,f't. when spec, fled in the No tice.
NEOSTIGMINE
NETILMICIN
NICOCODINE when compounded with one or ",ore other medicaments:"
(a) In divided preparaClons containing not more than lOOn,g of nicocodine pee dosage unit, or
(b) in undivided preparations with a concentration of not more than 2.5 per cenl of nicocodine.
NICODICODINE when corr,pounded lwi.th one or mor·e other medicaments:
(a) in divided preparations contai·ning not more than lOOn,g of nicodicodine per dosage unit, or
. .(b) in un4ivided preparations wlch a concentration of nOL more than 2.5 per c~nt of ni.codicodine.
. .. /23.
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- 23 -
NICOTINE in chewing tablets conta~ning 4~.g or less of nicotine per tablet for use. as an aid in wi.thdrawal fro(f, tabacco smoking.
NICOTINIC ACID for burr,an therapeutlc usee.~<::~p.E: in preparat ions containing 25()r,g or less of nicotinic acid per recommended daily dose.
NICOTINYL ALCOHOL for internal use.
NICOUMALONE for ioteral therapeutic use.
NIFEDIPINE
NIFENAZONE
NIKETHAMIDE
NIRlDAZOLE
NITRAZEPAM
NITROFURAN and its derivati.ves for bUlLan therapeutic use"~~,,e1:: when included in Schedule 2.
NITROUS OXIDE for therapeut ic. 4""e ' ..
NOMIFENSINE
NORADRENALINE (excluding its derivatives)
NORCODlUNE when corr.pounded with one or IT,ore other medicaments:
(a) in divlded preparations containing not more than lOOmg of norcodeine per dosage unit, or
(b) in undivlded preparations with a concentration of not IT,ore than 2.5 per cent of norcodeine,
"X.c:.e.EE: when included in Schedule 1.
NORETHANDROLONE
NORFLOXACIN
NORTRIPTYLINE
NOVOBIOCIN "x.<::"p.~ when specified in the Notice.
NYSTATIN
OCTAMYLAMINE
OCTATROPINE
OLEANDOMYCIN ~~S".p.~.:
•.• /24.
- 24 -
(a) when specif,ed in the NotIce. or
(b) in an i'f,a1 feeds for growth promot ion containing 5Or.g/kg or less of antibiotic substances.
0P:':PRAMOL
ORClPRENALINE
ORGANOPHOSPHORIIS COMPOUNDS with anticholinesterase activity for hurr.an therapeu
tic use ~~.::~e£;
(a) when included in Schedule 1; or
(b) when separately specified in this Schedule.
OENIDAZOLE
o RNIPRESSIN
o RPHENADRINE
CBTHOCAINE
ORTHOPTERIN
nXf",NDROLONE
OXAZEPIIM
OXPRENOLOL
OXYBUPROCAINE
[) ::r:'MESTERONE
OXYMETHOLONE
O)(Yl'HENBUTAZONE
,nYPHENCYCLIMINE
o XYPHENONIUM
()XYTETRACYCLINE ,='.'~~p.!:; when specified in the Notice.
i:'XYTOCIN
P I.HAQlJINE
iANCURONIUM
?LFcACETAMOL when corr.bined with aspirin. caffeine or salicylamide or any c1erivative of these substances.
._./25.
)
)
)
- 25 -
PARALBEHYDE
PAROMOMYCIN
PEMOLINE
PEMPlDINE
d-PENICILLAMINE
PENTAMETHONlUM
PENTHIENATE
PENTOBARBITONE when packed and labelled for injection.
PENTOLINlUM
PERHEXILENE
PERICYAZINE
PERPIiENAZINE
PHENACETIN for therapeutic use.
PHENACEMlDE
PHENAZONE ,,~~<:p~ when included in Schedule 1.
PHENAZOPYRIDINE
PHENETHICILLIN ".,,~ep~ when specified in the Notice.
PHENFORMIN
PHENGLUTARIMlDE
PHENINDIONE for internal therapeuttc use.
PHENIRAMINE <:~~"p.~ when included in Schedule 1 or 2.
PHENOXYBENZAMINE
PHENOXYMETHYLPENICILLIN ",,<:e.eL. when specifled in the Notice.
PHENSUXUlIDE and other substances structurally derived frotT, succinamide with anticonvulsant properties when used for therapeutic purposes.
+PHENTERMINE
PHENTHIMENTONlUM
PHENTOLAMINE
PHENYAPIN
PHENYLBUTAZONE
PHENYLEPHRINE in preparalions for hutT,an ophthalmic USe containing 5 per cent or IT,ore of phenylephrine.
PHENYLPROPANOLAMINE ~,,~~p~ when included in SChedule 2.
. .. /25.
- 26 - , ,
PHENYLTOLOXAMINE ~,,~ei'c when included in Schedule 2.
PHENYTOIN and other substances slructurally derived frorr. hydantoin with anticonvulsant properties when used for therapeutic purposes.
PHOLCODINE \.,hen corr.pounded WiLh one o[ IT,ore other rr,edlcarr.ents;
(a) in divided preparaLions containing not rr.ore than 100ng of pholcodine per dosage unit, or
(b) in undivided preparations wiLh a concentration of' not morE! than 2.5 per cent of pholcodine.
~!,~~p,~ when included in Schedule 1.
PHYSOSTIGMINE
PICROTOXIN
PILOCARPINE ~~~~PE. in preparations contalning 0.025 per cent or less of pilocarpine.
PIMOZIDE
PINDOLOL
PIPENZOLATE
PIPERACILLIN
PlPERIDOLATE
PIPOBROMAN
PIPRADROL
PIRENZEPINE
PIROXICAM
PITUITARY, its extracts and aCllve principles or thei.r synthetic substitutes ,,~c:~.!~t when separately specified in this Schedule_
PIZOTIFEN
PODOPHYLLUM RESIN (Podophylli.n) for hurr.an therapeutic use ~"c.<:eE, when lncluded in Schedule 1 or 2.
POLYMETHYLENE BISTRIMETHYL AMMONIUM COMPOUNDS
POLYMYXIN
POLYSULPHATED GLYCOSAMINOGLYCANS in preparatlons for injection, except where otherwise specified in this Schedule.
POTASSIUM PERCHLORATE for therapeutic use.
PRACTOLOL
... /2 7.
)
I
)
• )
)
)
- 27 -
PRA~lOXINE "',,~~['.~ when included in Schedule 1-
PRAZEPAM
PRAZOSIN
PREGNENOLONE ACETATE "',,"'~f'~ in preparaLions for topical use.
PRENYLAMINE
PRILOCAINE
PRIMAQUINE
PRIMIDONE
PROBENECID
PROBUCOL
PROCAINAMIDE
PROCAINE
PROCARBAZINE
PROCHLORPERAZINE
PROCYCLIDINE "'~~~.!'': when included in Schedule 1.
PROGUANIL
PROLINTANE
PROMAZINE
PROMETHAZINE ",,,<:~!'.t:. when included in Schedule 1 or 2.
PROPANIDID .
PROPANTHELlNE ~~c:"f'~ when included 10 Schedule 1 .
PROPRANOLOL
PROPOFOL
PROPOXUR for hurr,an therapeutic use,
PROPYLHEXEDRINE "~~"'!'.~ when included 1n Schedule 1.
.PROPYHENAZONE
PROQUAZONE
PROSTAGLANDINS ""C:"P.~ where separat:ely specified in t:his Schedule.
... /28.
- 28 -
+PROSTIANOL
PROTHIONAMlDE
PROTlRELIN (thyrotrophin releasing faclOr).
PROTRIPTYLINE
PROXYMETACAINE
PSEUDOEPHEDRINE in preparacions for stirr,ulant, appetite suppression'· or weight control purposes.
PYRIDOSTlGMINE
PYRIDOXINE HYDROCHLORIDE in preparat ions for hUIT,an use containing more than 5()r,g of pyridoxine per recommended daily dose unless labelled with the warning s taterr,enc "\,ARNING - THIS HEDICA 11 ON dAY BE DANGEROUS WHEN USED IN LARGE AMOUNTS OR FOR A LONG PERIOD".
PYRIMETHAMINE
QUINETHAZONE
QUINIDINE
RANITlDINE
RAUWOLFIA SERPENT INA
RIFAi>lPICIN
RITODRINE
ROLl TETRACYCLINE
ROSOXACIN
SALBUTAMOL ~x..~!:et: when included in Schedule 2.
SALICYLAl'1IDE when combined with aspirin, caffeine or paracetamol or . any derivative of these substances.
SALINOMYCIN !:~<,:<:p..r.;
(a) whellspecified in the Notice, or
(b) in animal feeds containing bOmg/kg or less of anlibiot ic substances. "
SELENIUM <:~~.".e~;
(a) when specified in the Notice,
(b) as selenium arsenide in photocopier drums,
(c) .in. ani'"al feeds containing O,.1g/tonne or less'of .se'leni\.ur.,
(d) in corr,pcessed pellets for cont:rol of selenium cesponslVe conditions in sheep or cattle. or
(e) in ferUlizers COntaining 200g/tonne or less of seleniurr •.
I~ a
'.
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)
.J
- 29 -
SEX HORMONES and ail substances having sex hormonill- activity ,::!!~"pt. when separately specified in these Schedules.
+SILVER SULPHADIAZINE
SISOMYCIN
SODIUM CELLULOSE PHOSPHATE for human internal use.
SODIIJH CROMOGLYCATE ,:::<~,,::P~ when included in Schedule 2.
SODIUM NITROPRUSSIDE for human therapeutic use,
SODIUM VALPROATE
SONTOQUlNE
SOTALOL
SPARTEINE
SPECTlNOMYCIN
S PIRAMYCIN ,,~<oep~;
(a) when specified in the Notice, or
(b) in anirr.al feeds for growth promotion in pigs or poultry contalning 50mg/kg or less of ant ibiot ic substances-.
SPIRONOLACTONE
SPUTOLYSlN _ See trans_4_(3,5_bibrorr.a_2_hydroxybenzyl)-arr.ino cyclohexanol hydro
chloride rroonohydrate.
STANOLONE
STANOZOLOL
STREPTOMYCIN "~~,,,e,~ when specIfied in the Notice.
STROPHANTHUS and ies glycosides •
STRYCHNINE in preparations containing, 1.5 per cent or less of st.rychnine for tbe
treatment of animals.
SULFAMETROLE
SULINDAC
SULPHANILAMIDE and its derivatives ,::~~"e~:
(a) when specified in the Notice,
(b) when separately specified in tbi.s Schedule,
.! •. /30.
- 30 -'t'
••
(c) oryzalin;
(<)) sulphaquinoxallne in animal feeds containing 20Orr.g/kg or less of sulphaquinoxaline, or
(e) sulphaqulUoxaline when incorporated in baits for the destruction of ve rrr.i n.
+SULPHAIROXAZOLE
SULPHINPYRAZONE
SULPHOMYXIN
SULPHONAL and alkyl sulphonals,
SULTHIAME
SUXAMETHONIUM
TACRINE
TAMOXIFEN
TEMAZEPAM
TENIPOSlDE
TERBUTALINfj; ,,~~£\:.t when included in Schedule 2 ,
TERFENADINE
TEROPTERIN
TETRABENAZINE
TETRACOSACTRIN
TETRACYCLINE ~~C.~E~ when specified in the Notice,
+THALIDOMIDE
THENYLDIAMINE ~'.',"'7..E": when included in Schedule lor 2,
. -
THEOPHYLLINE ~'.'c."e!;,when included in Schedule 2',
THIACETARSAMIDE, in preparations for the prevention or treatrr.ent of heart worm in dogs,
THIACETAZONE
THIAMBUTOSINE
THIAZOSULPHONE
THIETHYLPERAZINE
THIOPROPAZATE
THIORIDAZINE
... /31.
,
'"
')
- 31 -
THIOTEPA and other substances strucLurally derived therefrorr. with cytotoxic properties when used for therapeutic purposes.
THIOTHIXENE
THIOURACIL and substances slructurally derived therefrolT. w.lth amithyroid properties when used for therapeuti.c purposes.
THIOUREA for therapeutic use,
THYROID and extracts, and ies acr.ive prinCiples eX~"l?~ when separately specified in this Schedule.
THYROTROPHIN (T.S.H.)
THYROXINE SODIUM
TIAMULIN ~~c.:~e,~;
(a) when specified in the NOLice.
(b) in prepared aom.al feeds.
TICARCILLIN
TIEl~ONIUM
TIGLOIDINE
TIMOLOL
TINlDAZOLE
TIOCONAZOLE ~~~.ee~ when in Schedule 2.
TIPEPIDlNE
TOBRAMYCIN
JOCA):NIDE
TOLAZAMIDE
,J . TOLAZOLINE Eor ,internal use.
TOLBUTAMIDE
TOLPROPAMINE
) TRANEXAMIC ACID
TRETAMINE
TRIAMTERENE
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TRIAZIQUONE
TRIAZOLAM
TRICHLOROETHYLENE for therapeut i.c use.
TRICLOFOS
TRICYCLAHOL
TRlDlilEXETHYL
TRIFLUOPERAZINE
TRIFLUPERIDOL
TRIHEPRAZINE ,:!'~~e,t. when included i.n Schedule 1 or 2.
TRIHETAPHAN
TRIMETHOPRIM
TRIMIPRAHINE
TRIMUSTlNE
TRIOXYSALEN
TRIPELENNAMINE
TRIPROLIDlNE ~?::~~p..~ when included in Schedule 1 or 2.
TROXIDONE and other subscances structurally derived frorr, oxazolidinone with anticonvulsant properties when used for therapeutic purposes.
(a) when i.ncluded Ln the NOllce.
(b) in anirr,al feeds for growth promotion containing 5Qrr,g/kg or less of antibiotic substances. or
(c) in milk replacers for calves Or starter rationS for pigs, . contai.ning lOOmglkg Or less of antibiotic substances.
URETHANE (excludlng iLs derivatives) fot therapeutic use.
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URETHANES AND UREIDES having or purportIng to have soporific, hypnotic or narcotic properties !!~!et when separately specified in these Schedule.
VACCINES, se ra, toxo ids, and ant igens for hurr.an parentera I une.
VACCINES, veterinary live virus e!,::!p,::;
(a) poultry vaccwes.
(b) pIgeon pox vaccine, or
(c) scabby mouth vaCC1ne.
VALNOCTAMlDE
VASOPRESSIN
VERAPAMIL
VERATRUM for therapeutic use.
VECURONIUM
VlDARABINE
VINCA ALKALOIDS includlng serr,i-synthellc derivatives.
VIPRYNIUM
VISNADINE
(a) when specifled in the NoUce, or
(b) i.n animal feeds for growth pron.otion conta1ning 5()r,g/kg or less of antibiotic substances.
VITAMIN A for hUIT,an tr,erapeut!c use, except 1n preparat ion containing 10 000 l.U. or less of vitarr.in A per recorr,mended--da-(ly dosage.
VITAMIN D for human therapeutic use except in preparations containing 25 tr,icrogr.ams or less of vitaQ",in D per recomrr,ended ~aily dosage~
WARFARIN for internal therapeutic use.
XANTHINE OXIDASE INHIBITORS includIng allopurinol.
XANTHINOL NICOTINATE
XYLAZINE
YOHIMBINE
ZERANOL !!c::."PS when specified in the Notice.
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2.
3.
4.
5.
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7.
8.
9.
10.
11.
12.
13.
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REPUBLIC OF VANUATU
THE FIREAl.'l.MS REGULATIONS No. 27 OF 1988
Arrangement of Sections
Interpretation.
Form of application for firearm licence.
Form and conditions of firearm licence.
Form of application for a firearm dealer's licence.
Form of firearm dealer's licence.
Particulars to be entered in the register of the licenced firearms dealer.
Requirements for a firearms dealers'S licence.
Form of application for a firearms import licence.
Form of firearms import licence.
Register of firearm importers.
Lost licences.
Disposal of deposited, detained and forefeited firearm ammunition.
Vol.untary deposit of firearms and ammunition in police armouries.
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14.
15.
Fees.
Commencement.
Schedule I
Schedule 2.
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REPUBLIC OF VANUATU
THE FIREARMS REGULATIONS No. 27 OF 1988
To provide for the forms, fees and other matters connected therewith for the purposes of the Firearms Act No.7 of 1987.
IN EXERCISE of the powers conferred by section 42 of the Firearms Act No.7 of 1987, I HEREBY make the following regulations:-
INTERPRETATION 1. In these regulations, unless the context otherwise requires:
"Act" means the Firearms Act No.7 of 1987;
"Licensing Officer" means a licensing officer appointed under section 2 of the Act.
FORM OF APPLICATION FOR FIREA&~ LICENCE 2. (1) An application for the grant of a firearm licence under
subsection (1) of section 9 of the Act shall be made to the licensing officer of the area in which the applicant resides in Form 1 in Schedule 1 hereto.
(2) An application for the renewal of a firearm licence under the Act shall be made to the licensing officer in Form 1 in Schedule 1 hereto.
FORM AND CONDITIONS OF FIREARM LICENCE 3. (1) Every firearm licence granted under subsection (4) of section
9 of the Act -
(a) shall be in Form 2 set out in Schedule. 1 hereto;
(b) shall contain the certificate in Form 3 set out in Schedule 1 hereto; and
shall be subject to the following conditions:-
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(a) the firearm and ammunition in respect of which the licence is granted shall at all times when not in actual use be kept in a secure place with a view to prevent use or access to them by any person not lawfully entitled to use them~
(b) the loss or theft of any firearm to which the licence relates shall be at once reported to the nearest police station or licensing officer;
(c) except as the licensing officer otherwise permits, the firearm and ammunition shall be kept at the permanent address of the ho Ider of the firearm licence and the licensing officer shall be notified in writing within 14 days of any change of such address and of any change in the address at which the holder of the licence is otherwise permitted to keep the firearm and ammunition;
(d) the holder of the licence shall obey all lawful orders of any police officer or licensing officer relating to -
(i) the licence; (ii) any firearm or ammunition possessed or acquired
under the 1 icence :;
and shall produce such licence~ firearm or ammunition to such officer on demand;
(e) the firearm or ammunition in respect of which the firearm licence is granted shall not be used for any unlawful purpose.
(2) Every certificate given to the holder of a firearm licence shall be retained by him for production to the licenced dealer or~ if required 9 to a police or licensing officer.
FORM OF APPLICATION FOR A FIREARM DEALER'S LICENCE 4. An application for the grant of a firearm dealer's licence
under subsection (2) of section 9 of the Act shall be made to - the licensiiig- officer in Form 4 in Schedule 1 hereto.
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FOHH OF FIllliAl<i'1 DEALER'S LICENCE 5. Every firearm dealer's licence granted under. section 11 of the
Act shall be in Form 5 in Schedule 1 hereto and shall be subject to the following conditions:-
(a) that the holder of a firearm dealer's licence or his servants emp toyed in the ordinary course of business of such holder as a licensed firearms and ammunition dealer, shall observe the provisions of the Act and of any regulations made hereunder;
(b) that the holder of a firearm dealer's licence or his servants employed as aforesaid shall not part with possession of any firearm or ammunition except to a person lawfully entitled to possess the same;
(c) that the holder of a firearm dealer's licence servants employed as aforesaid shall obey all orders of any police or Licensing officer relating firearm or ammunition in their possession;
or his lawful to any
(d) that any firearm and ammunition in the possession of the . holder of a firearm dealer's licence shall not be used for any unlawful purpose;
(e)· that the holder of such licence shall ensure that the proper records required under the Act and the Regulation are maintained by him in the prescribed form.
PARTICULARS TO BE ENTERED IN THE llliGISTER OF THE LICENCED FIREAHHS DEALER 6. (1) Every licenced firearms dealer shall enter or cause to be
entered in the register of transactions required to be kept under section 11(6) of the Act, the following particulars:-
(a) the quantities and description of firearms and ammunition purchased or acquired with the names and addresses of the sellers or transferors and the dates of the several transactions;
(b) the quantities and description of firearms and ammunition sold or transferred with the names and addresses of the ~
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purchasers and transferees (except in cases where the purchasers are transferees), the areas in which firearms were sold or transferred and the dates of the several transac,_t ions;
(c) the quantities and description of firearms and ammunition accepted for sale j repair~ tests proof, cleaning, storage, or other purpose, with the names and addresses of the transferors and the dates of the several transaction;
(d) the quantities and description of firearms and ammunition in possession for sale or transfer at the date of the last stock-taking or such other date in each year as may be specified in the register.
(2) The register shall be kept in three books and shall be in Form 6 in Schedule 1 hereto.
(3) Every licenced firearms dealer shall, between the 1st and 7th of each month furnish particulars under section 11(8) of the Act, to the licensing officer in Form 7 in Schedule 1 hereto.
REQUIREMENTS FOR A FIREARMS DEALER'S LICENCE 7.. Every licenced firearms dealer selling
possession of a firearm or. ammunition to firearm licence shall -
or parting with the holder of a
(a) fill and sign the certificate of transaction in Form 3 in Schedule 1 hereto;
(0) within 48 hours from the transaction, send a copy of the Certificate of the transaction to the licenSing officer;
(c) in any case report in writing 48 hours to the licensing officer any circumstances attending the transaction which appear to require investigation.
FOR?'! OF APPLICATION FOR A FIREARMS IMPORT LICENCE 8. An application for the grant of a firearm import licence under
subsection (1) of section 14 of the Act shall be made to the licensing officer in Form 8 in Schedule 1 hereto.
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FORM OF FIREARMS IMPORT LXCENCE 9. Every firearm import licence granted under section 14 shall be
in Form 9 in Schedule 1 hereto.
REGISTER OF FIREARI'1 IMPORTERS 10. A licensing officer shall, under subsection (2) of section 14
of the Act, keep and maintain a register which shall be in Form 10 in Schedule 1 hereto.
LOST LICENCES 11. (1) Any person who ·having obtained a replacement licence under
section 15 of .the Act, in place of the licence he has lost, finds such lost licence shall within 10 days of finding the licence, surrender it to the licensing officer or a police officer.
(2) Any person who contravenes this regulation shall be guilty of an offence a"nd liable to a fine not exceeding 10,000 vatu or to imprisonment for a period not exceeding two months or to both s.uch fine and imprisonment.
DISPOSAL OF DEPOSITED, DETAINED AND FORFEITED FIREARM OR Al1MUNITION 12. (1) Any firearm or ammunition detained under the provisions of
section 20 of the Act shall, at the expiry of the period of detention, unless previously brought before any court, be returned to the persons Lawfully entitled to receive the same. If there is no such person, such firearm or ammunition may be sold or disposed afas the Commissioner of Police deems fit •
. (2) Any firearm or ammunition deposited at a police station or police armoury in accordance with the provisions of subsection (1) of section 37 of the Act, if not taken possession of by the lawful owner in accordance with the provisions of subsection (2) of section 37 and not disposed of in the
.manner specified by that subsection, shall be disposed of as the Commissioner of Police deems fit.
(3) Where any firearm or ammunition is detained under the provisions of section 36 of the Act and at the expiry of the perio-d of detention, such firearm O-T ammunition cannot be returned to the person lawfully authorized to receive the same in accordance with section 38 as such person cannot be found,
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such firearm or ammunition may be sold or disposed of as the Commissioner of Police deems fit.
(4) Firearms and ammunition forfeited in accordance with the provisions of section 39 of the Act may be sold or disposed of as the Commissioner of Police deems fit.
(5) If any police officer in charge of a police armoury considers any firearm or ammunit·ion deposited or detained therein in accordance >lith the Act or these Regulat ions to be in an unsafe condition, he shall report the unsafe condition of such firearm or ammunition to the Commissioner of Police who may cause. such firearm· or ammunition to be destroyed in such manner as he deems fi t~
(6) The proceeds from the sale of any firearm or ammuntiion re.ferred to in this regulation, other than the proceeds of sale under sectionJ37,~haI1 be paid into the Treasury.
VOLUNTARY DEPOSIT OF FIREARMS AND AMMUNITION IN POLICE ARMOURIES 13. (1) Any person in lawfull possession of a firearm or ammunition
may deposit such firearm or ammunition in a police armoury for 'safe custody.·
FEES.
.(2) It shall be the duty at the officer in charge of the armoury to take reasonable care of all firearms and ammunition so deposited, but notwithstanding any breach 6f duty or the negligence of any police officer or otherwise, no action shall lie' against the Government or any police officer in respect of the loss of or damage to any firearm or ammuniton so
. deposited.
14. (1),. The fee payable .inrespect of any licence referred to in the Act, and in respect of any deposition of firearm in police armoury. or of. variation- of conditions in firearm licences shall be the fees respectively specified in Schedule 2 and shall be paid to the licensing officer.
(2) Any· fee payable on the grant of a licence, renewal of a lic.ence, variation of conditions ,ina licence or deposit of firearm .in pol ice armoury shall be paid before the applicant -
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is granted a licence s renewal ~ variation of conditions or deposit of firearms s us the case maybe.
COMMENCEMENT 15. These regulations shall come into force on the date of their
publication in the Gazette.
MADE at Port Vita, this ,1st day of
IOLU J ABBIL Minister of Home Affairs
July , 1988.
SCHEDULE I
FORMS
FORM 1 (regulation 2)
THE FIREARMS REGULATIONS
FORM OF APPLICATION FOR A. FIREARM LICENCE
1. Name in full .................................................................................................. ..
2. Full postal address - Village/Town ................................................. t ......... ..
Island.'". ••• ~.; •••••••••••••••••••••••••••••••
3. Age ............................... 4. Nationality ............................................................ ..
5. Occupation ............................. 6. Employer ................................................ ..
7. Business address .................................................................. , .....................................................................................................
8. Description of firearm for which licence required ..•..••..••.....•.
9.
.. .. .. .. • .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 0·0 ............................................................. .
(a) Details of firearms possessed at date of application ••••••••••
. . . . . . . . . . . . ~ ................................................ . (b) Ammunition-
Quantity
Possessed at date of application ••••.••
Calibre and Type
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(ii) Total amount desired to be purchased
or acquired in one year
(iii) Ha"imum amount desired to be ?ossessed
or acquir'e.d a t a ny one time ......... ..
10,. Whether' 'a lke'nc'e has previously' been held, or' applied for by applicant. If so, give details of all previous applications •••••••
. . . . . .. . . . . . .. . .. . . . . . . . . . .. . . . . . . .. . . . . . . . . . . . . . . . .. . . .. . . . . .. . .. . . . . . . .. . . . 11. Date and place of issue of any licence to possess firearms or
ammunition held' during' previous 3 years ............................... .
. . . .. . . . . . . . .. . . . . . . . . .. . .. . .. .. . . . . . . . . . . . . . . . .. .. .. . . . . . .. . . . . .. . .. .. . . . . . . . . .
12.' Do you suffer from any form of mental disorder or defect?
YES/NO. If YES, give details: ............................... ......... .
13. Have you been convicted of any offenc~1 other than minor traffic offences. ,YES/NO.
If YES 9 gi va details: ............................................. .
14. Reasons for requiring each of the firearms and ammunition . . specified:· 0· ••••••••••••••••• c ................................. .- •••••••••••
15. Where do you intend to use each of the fire,arms specified?
16. Where ~ if a firearm licence is· gra.nted will each of the firearms and the ammunition sp3cified be kept when not in use?
DECLARATION
I hereby apply for a licence in respect of the firearm(s) and ammunition specified above~ and 1 declare that the statements made above are true and complete in all respects.
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Da t e •••••••.•••.••.• Signature ......................... ..
For Official Use
Th:i.s application was lodged at .. to ............................ (office)
on (date) ......•.......... o ••••••••••••••••• _ ••••••••••••••••.•••••••
'RECOMl1ENDED/NOT RECOMMENDED
Reasons for non-recommendation ............................. I ••••••••••••
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . LICENCE Approved/No~ Approved AHMUN1TlON
(i) maximum amount author,ised to be possessed at anyone time*-
........................................................... (ii) total amount to be purchased in each 'year*-
........................................................... *State quantity, type and calibre
Da'te' •.•.••••••.•••••.•••••••• Signa,ture ............•..........• Licensing Officer
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FORH 2 (regulation 3)
THE FIREARMS REGULATIONS
FIREARM LICENCE
LICENCE NO ••••••• -••• ' ••• ' ••• '.
Full Name •••••••••••••••••••••••••••••• ~ ••• , ••••••••••••••• •••••••••••••• (Block Letters)
Vi.llage/Town ........................................................... .
Island .......... 0" ....................................................... .
is hereby authorised to possess the firearm(s) and ammunition specified hereunder
(a) Firearm
( i) Type •••••••••••••••••••••••••••.•••••••.••••••••••••
(ii) Cal ibre ..................•.........•.....•.....•.....
(iii) 11ake r I a Name •••••••.•. ' •••••••.•••••••••••••••••••••••
(iv) iYlaker's Number ••• 10 •••••• O. 00 00 ••••••••••••••••••••••
(b) Ammunition-
(i) maximum amount authorised to be possessed at anyone time.;" ................................................ .
(ii) total amount authorised to be purchased in each year, comme.ncing 19 ....... "''' .................................. .. .................................................................... * State quantity, type and calibre.
The following conditions shall be observed by the holder of this 1. icenc€:-
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(1) the firearm(s) and ammunition to which this licence relates shall at all times when n'at in actual use be kept in a secure place with a vi.m'] to preventing use or access to them by persons not entitled to use them,
(2) the loss or theft of any of the firearm(s) or ammunition to which the licence relates shall be reported at once to the nearest police statio'fl or licensing officer.;
(3) except the licensing officer otherwise permits, the firearm(s) and · ammunition shall be kept at. tl;1e permanent address of the holder of this licence and the licensing officer shall be notified in writing "ithin .. , •• ,.of, any change of SUC!! address and of any change in the address at which the holder of .this licence is otherwise permitted to keep the firearm(s) or ammunition;
(4) the, holder of this licence shall take all necessary steps to secure th8,t regulation 5 of the Firearm" Regulation (which relates to instructions con~erning the sale or transfer of firarms and ammunition by licensed dealers) is complied with;
:, (5)·· the holder of this licence shall obey all lawful orders of any police officer or licensing officer relating to the licence, or any
· fi: ..... earm or ainmunition possessed or acquired under this licence and ,shall p~oduce.such licen~e firearm or ammunition to such officer on demandt
(6) that such firearm or ammunition shall not be used for any unlawful · purpo.se s.
The licensing' office'r 'inay 'insert any 'other condition herebelow:
This licence" shall reamin in fo~ce unt11 •••••. ~.~ ••.••••••••.••••••••.•• unle~s previously revoked or cancelled.
Date: ....•........••••...... Signature: ........................... . (Licensing Officer)
T.R. No .... o ••••••••• '0,0"
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A
Date of sale or transfer
FORl1 3
THE FIREARMS REGULATIONS
CERTIFICATE
TABLE 1 (FIREARMS)
B
Name and address of person selling or transferring firearm
C
Quantity, Calibre, make and type of firearm identification number or other mark
(regulations 4)
D Certificate
I certify that the entries in columns A to C are correct and relate to a transaction and I have satisfied myself that the transaction wi 11 not place the holder of the licence in possession of firearmS in excesS of or otherwise than as authorised by the licence.
Signature ..•...... I
Date: .............. .
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RENEWALS
This licence is hereby renewed and is valid until •••..•..••....••• 19 .•. ,
unless previously revoked or cancelled.
Date ...•..... """" .•. """." " Sig~ature """."""""""""""""""""",,.,," Licensing Officer
T.R. No ••. " ."."."
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FORM 4 (regulation 4)
THE FIREARMS REGULATIONS
FORM OF APPLICATION FOR A FIREARMS DEALER'S LICENCE
1. Name in Full ...•...•...•........•.•.....•.. ' ......................... .
2. Addre,;ssO"o .............................................. ,; •••••••••••••••
3. _Intended' 'Place of Business ........•...•...........•..•.............
4... Description of Firearms and Ammunition for which a ,required -
licence is
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5.
. (a) Firearms State Make, Type, Calibre and Maximum Quantity to . be. held at anyone time - ..........•........•......•...•......
· ... .. ' ......................................................... . . t' ............................................................. .
(b) ill.munition - State Make, Type, Calibre and Maximum Qunatity to
(a)
be held at anyone time - ................................... .
t' .................................................................................. "' ... ..
.............................................................................................................
State for •
"hethel" a licence .has previQusly been held or If so, give dates of all previous applications.
applied
.. .. .. .. .. . . ,. ............................................................................. .. · ................................................................................................ .
(b) Date and place of issue of any licence to deal in firearms and ammunition held during previous 12 months .•.•••.••.•.••.•••..•
· .......................................................................................................... .
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A
Date of sale or transfer
B
Name and address of person selling or transferring -ammunition
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TABLE 2 (AMMUNITION)
C
Quantity of ammunition
D
Calibre and description of ammunition
E Certificate
I certify that the entries in columns A to D are correct and relate to a transaction with the holder of this licence, that I have inspected this licence and the record of previous transactions and I have satisfied myself that the transaction will not place the holder of the licence in possession of a.mmunltion in excess of or otherwise than
. as .authorised by the licence.
Signature: .......... '.'.-.'
Date:.: .' ....... .: •• .- .• '.' ••••
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FORl1 5 (regulation 5)
THE FIREARM REGULATIONS
FIREARM DEALER', S LICENCE
LICENCE No: ........ ~ .' ......... o. ... .
This licence authorises .... e,.o..o. .... o. .. o. ,"o. ...................................... ., ~ ~ .... ~ ............ o.
of ...................................................................................... In the Republic of Vanuatu or his servants in the ordinary course of his business as a licensed firearms and ammunition dealer -
(a) to assemble or disassemble, clean, repair, test or approve any firearm or'ammunition;
(b)' to manufacture any component part of a firearm or ammunition;
(c) to sell, transfer or expose for sale any firearm or ammunition;
(d) to keep or any of the
have in their possession aforesaid purposes at the
any firearm or ammunition for foll,?wing place(~) - ~ ••••••••
•••••••••••••••••••••••••••••••••••••••••• 1 ••••••••••••••••••••••••
This licence is subje.ct to the following conditions -
(1) that the holder of such licence or his servants employed .in the ordinary course of business of such holder as a licensed firearms and ammunition dealer, shall observe the provisions ofthe.Act and.of any regulations made hereunder;.
(ii) that the holder of such licence or his servants employed as aforesaId sha 11 not part with possession of any firearm or ammunition except to a person lawfully entitled to possess the same;
(iii) that the holder of such licence or his servants employed as aforesaid &hall obey all lawful orders of any police or licensing officer relating to any firearm or ammunition in their possession;
••• /2.
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DECLARATION
I hereby apply for a licence to deal specified above and 1 declare that the and complete in all respects.
in the firearms and ammunition statements made above are true
Date .... ' ... ~' •.... ~ .. _.; ..... Signature of Applicant ..•.......•• .: ......... .
For official Use
This a'ppiication was lodged at . ' .......................... ,_ ... (office)
on (date) .....................•.....•....•...... -.' .........•....•.....•..
RECOMMENDED/NOT RECOMMENDED
Reasons for non-recommendation .......................................... .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. . . . . . . . . . . . . . . . . . . . ' ......... .
LICENCE Approved/Not Approved
Date ...................... ' ...... . Signilture ................... . Licensing Officer
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FORM 6 (regulation 6)
FIREARMS REGULATIONS
DEALER'S REGISTER OF TRMiSACTIONS
TABLE 1 - FIREARMS
(A separate' folio to be used for each type of firearms)
Type ~ .- .... ~ • " •• ," ... -e,." ........ i .... ........ Ii ..
ACQUISITION
S~urce '(in case of import state
.country), and ,full name and address of firm or person
from whom acquired
Name and
Make, calibre and identity No.
DISPOSAL
address of person to whom sold or supplied
No. and date of ,import licence
Make" ' calibre and and quantity sold or. disposed of and identity No.
Quantity
Balance in stock
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(iv) that any firearm and ammunition in the possession of the holder of such licence shall not be used for any unlawful purpose;
(v) that the holder of such licence shall ensure that the proper records required under the Act and the Regulation are maintained by him in the prescribed form;
('Ii) Additional ~on~iti9PS ...... ," 01' ~ ~I"""""""""""""'"
................................ , .......................... .
This licence shall 'con"tiiiue"'fn---force until ...•.....••..•.....•. , 19 ..•. unless previously revoked or cancelled.
Da t e ..................... . Signature ........ , .' .................. . Licensing Officer
T.R. No ......... .
RENEWALS
This licence ishereby renewed ,and shall remain in fo~ce until.., .. " ....
•••••••.•••••••••••. 19 •••• ~ unlesn previously revoked or cancelled.
Date: .........•.•........ Signature: ... I •••••••••••••••••
(Licensing Officer)
T.R. No: ....• ,,' ..•...•...
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TABLE 2 - AMMUNITION
Calibre ••••• , ••• ; •••• (A separate folio to be used for each calibre of Ammunition)
Date
Date
ACQUISITION
Source (in case of import state countl-Y), and full name and addres.s of firm. or person from whom acquired
Make, type and quantity received
DISPOSAL
Hake, type and quantity sold
Name and address of person to who'm sold
Number and date of Import Licence
Balance in Stock
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TABLE 3 - REPAIRS, ALTERATIONS, STORAGE, TESTING, ETC ..
1 2 3 4 5
Make, type, Full name calibre and QuantUy and
Date and address ROlasonfor identity calibre of . of depositor depositing markings of ammunition
firearms or deposited component part deposited
\ 6 7 8 9 )'
\ Firearms licence No. By whom date and station
Date removed of issue Remarks Removed (fulJ name produced by ,
and address) person removing
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FORM 7 (regulaltion 6(3))
THE FIREAMRS REGULATIONS
RETURN OF FIREARMS AND Al~NITION PURCHASED, IMPORTED. AND SOLD
(To be forwarded by licensed fi.rearm's dealers to the licensing officer between the 1st and 7th of each month)
Month of ...••.••.. 19 •••••••• ~ •
Stock in hand on
Purchased or imported* on .•...•.
11 11 ... '" ... " . "
Sold on II II
11 11 0' ••• ' •••••••
Balance in Stock on
TABLE 1 - FIREARMS
• 22 Rifles
12g • Shotguns
.410 Shotguns
Other Shotguns
1'Where imported also include Import Licence Number .
•.• /2 •
l"lonth of.', ••... -~' ••. 19 .......... .
Stock in hand on
...... , ............ .
Purchased or imp'oTt"ed';'\'" on •• 'j, .....
il H •••• • ,f •
II II
Sold on ........... II It ........... II 11
,Balanc,e.in stock, on
...................
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TABLE 2 - AMMUNITION
.22 Rifles
12g Shotguns
,,140 Other Shotguns Shotguns
*Where imported also record Import Licenc?Number
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5.
FORl1 8 (regulation 8)
THE FIREARl1S REGULATIONS
FORl1 OF APPLICATION FOR A FIREARl1 IMPORT LICENCE
Name in Full ................•........................•........•...
Address ............•.....................................•..•..•...
Place of Business .....................•......•......•.••.....•....
Description of Firearms and Ammunition desired to be imported -
(a) Firearms - State make, type, calibre and quantity of firearms
to be imported .•..•...•...........••...................•..•..•
• ..................................................... • ,0 ••••• 0'.
• ................................... t ..................... • ,", ••••
(b) Ammunition State make, type, cal ibre and quantity to be imported ...................................................... .
· .... ,. ,. . ,. ..... ,. ,. ,. ........................................................ .. · ........................... " ............... " ...................... " ..... ..
(a) State whether a licence has previously been held or applied for. If S0§ 'give dates of all previous applications ........................................ 0 .............. .
, ' ~
• • " .• , ••••• 0 •••• " .......................... 0 e·· ................. ,. ••••
· ,. ................................... .... ", .. " ............... " ..... . (b) Date and place of issue of any licence to import firearms and
ammunition granted during last 12 months .................•... . 0 ................................. " ...................... ,. .•••••••
6. Details of firearms and ammunition possessed at date of this application. (State quantity, make, calibre, type, serial No. or other distinguishing mark, and exporter). If none, say NONE.
••. /2.
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7. Reasons for requ~r~ng the firearms and ammunition specified above:
•••••••• ' ••.••••• ' •••• e.' .............. ', •••.•••••••••••••••••••• , •••••
• • • • • • • • • • • ~ •••••••••••••••••••• It •••••••••••••••••••••••••••••••••
DECLARATION
I hereby apply for a licence to imp'ort the firearms and ammunition specifie,d above. I am the holder of a Firearm Dealer I s Licence No .1* I declare that the statements made above are true and complete in all respects.
"Delete if inapplicable.
Date ............... ~ ..... : .. Signature of Applicant ...............•......
For. Official Use
This application 'was lodged at. ••.•.•••.••..••••••••••••••••••• (office)
, '.' , ,
on (date) ...............................................•.•.....•.......
RECOi~l~ENDEDiNOT REC0i111ENDED
Reasons foL:' non-r.ecommendation .••........•.... -. -. ......................•.
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . LICENCE Approved/Not approved
i)'ate ••.••• ~ ••.• " •••• " ••• ' Signature: •................... Licensing Officer
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REPUBLIC OF VANUATU
FORM 9 (regulation 9)
THE FIREARMS REGULATIONS
FIREARMS IMPORT LICENCE
LICENCE No .............. ..
Full Name ~ ••••••••••••••• •• ' ................ It' •••• " •••••••••••••••••••••••••••
Addre s s ....•....•••.•.....•.....•...•..•.•••.. .- .......... J .... ,'';'.'.'." .,'.' •• '" ... ' ..... '" , .•
is hereby Licensed to import into the Republic of Vanuatu firearms and ammunition of the number and description hereunder specified -
Quantity. Description Calibre Remarks
This licence shall continue in force until .............. 19 ........... . unless previously revoked or cancelled.
D2 te ................ . Signature ....................... . Licensing Officer
T.R. No .••. o 0 ••• t.
Name and place of business
FORM 10
FIREARHS REGULATIONS
REGISTER OF FIREARMS IMPORTERS
Date appli-. Date appli-cation cation received approvedi
not approv-· ed
Date licence issued
Licence No:
(regulation 10)
T.R.No. Date Renewed
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SCHEDULE 2
FEES
Particulars
1. Grant or renewal of firearm licence under section 9(2) of the Act.
2. Variation of conditions in firearm licence under section 9(8) of the Act.
3. Grant or renewal of firearm dealer's licence under section 11(3) of the Act ..
I,. Grant or renewal of firearm import licence under section 14(3) of the Act
5. Issue of replacement firearm licence under section 15 of the Act
6. Deposit of firearm in police armoury under section 37(1) of the Act.
(regulation 14)
Fees
3,000 vatu.
1,000 vatu.
30,000 vatu
500 vatu per firearm.
1,000 vatu.
1,000 vatu per firearm
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REPUBLIC OF VANUATU
THE FIREARMS ACT No. 7 OF 1987
NOTICE
IN EXERCISE of the powers conferred by section 17 of the Firearms Act No.7 of 1987, 1 HEREBY DELCAl;lE .-
(1)
(2)
That no firearms or.' ammunition whatsoever shall b·e imported into Vanuatu except at the Overseas wharf in Port Vila and Batterfield Airport in Port Vila;
That the follo"ing firearms and ammunition shall not be imported into Vanua tu:-
(a) automatic firearms, that is firearms which are so designed or adapted that if pressure is applied to the trigger, missiles continue to be discharged until pressure is removed from the trigger or the magazine containing the missiles is ernpty~
(b) semi-automatic firearms!, that. is firearms other than automatic firearms as specified in paragraph (a) ~ which when fired eject the spent round and refill the breach;
(c) pistols and revolvers of all types;
(el) firearms and ammunition of the following calibres:-
.300, .303, .38 and .45 inches, and 7.62 and 9 millimetres;
(e) any w,=apon of whatever descriptton designe.d or adapted for the discharge of any noxious liquid, gas or other thing; and
(0 any ammunition containing or designed or adapted to contain any such noxious thing .
. This NOTICE shall come into force on the date of its publication in the Gazette.
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HADE at Port Vila this 1st day of July, 1988,
lOLU J ABBIL Minister of Home Affairs
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