Poisons List Amendment Order (No. 3) 2008 (TAS)
Poisons List Amendment Order (No. 3) 2008
I make the following order under section 15(1) of the Poisons Act 1971 .18 December 2008
LARA GIDDINGS
Minister for Health
| 2054. | Fluorides for human use – |
| (a) in preparations for ingestion containing 0.5mg or less of fluoride ion per dosage unit; or | |
| (b) in liquid preparations for topical use containing 1 000mg/kg or less of fluoride ion, in a container with a child-resistant closure – | |
| (i) for therapeutic use when compliant with the requirements of the | |
| (ii) for non-therapeutic use when labelled with warnings to the following effect: | |
| (A) Do not swallow; | |
| (B) Do not use [this product/name of product] in children 6 years of age or less – | |
| except in preparations containing 220mg/kg or less of fluoride ion, in packs containing not more than 120mg total fluoride, when fitted with a child-resistant closure and labelled with warnings to the following effect: | |
| (A) Do not swallow; | |
| (B) Do not use [this product/name of product] in children 6 years of age or less – | |
| except in preparations containing 15mg/kg or less of fluoride ion or preparations for supply to registered dental professionals or by approval of an appropriate authority. |
| 3033. | Fluorides for human topical use – |
| (a) in liquid preparations containing 5 500mg/kg or less of fluoride ion, in a container with a child-resistant closure, except when included in or expressly excluded from Schedule 2 ; or | |
| (b) in non-liquid preparations containing 5 500mg/kg or less of fluoride ion except – | |
| (i) in preparations for therapeutic use containing 1 500mg/kg or less of fluoride ion and, when containing more than 1 000mg/kg of fluoride ion, compliant with the requirements of the | |
| (ii) in preparations for non-therapeutic use containing 1 500mg/kg or less of fluoride ion and, when containing more than 1 000mg/kg of fluoride ion, labelled with warnings to the following effect: | |
| (A) Do not swallow; | |
| (B) Do not use [this product/name of product] in children 6 years of age or less; or | |
| (iii) in preparations for supply to registered dental professionals or by approval of an appropriate authority. |
| 3039. | Glyceryl trinitrate in preparations for – |
| (a) oral use; or | |
| (b) rectal use. |
| 40042. | Alglucosidase. |
| 40207. | Boron, including boric acid and borax, for human therapeutic use except – |
| (a) in preparations for internal use containing 6mg or less of boron per recommended daily dose; or | |
| (b) in preparations for dermal use containing 0.35% or less of boron, which are not for paediatric or antifungal use; or | |
| (c) when present as an excipient. |
| 40432E. | Daptomycin. |
| 40722. | Glyceryl trinitrate except when included in Schedule 3 . |
| 40786M. | Idursulfase. |
| 40830M. | Ixabepilone. |
| 40846R. | Laropiprant. |
| 40853M. | Lenalidomide. |
| 40894E. | Maraviroc. |
| 40894R. | Maropitant. |
| 41077. | Nitric oxide for human therapeutic use. |
| 41220E. | Piper methysticum (Kava) in preparations for human use, except when included on the Australian Register of Therapeutic Goods in preparations – |
| (a) for oral use when present in tablet, capsule or teabag form that is labelled with a recommended maximum daily dose of 250mg or less of kavalactones and – | |
| (i) the tablet or capsule form contains 125mg or less of kavalactones per tablet or capsule; or | |
| (ii) the amount of dried whole or peeled rhizome in the teabag does not exceed 3g – | |
| and, where containing more than 25mg of kavalactones per dose, compliant with the requirements of the | |
| (b) in topical preparations for use on the rectum, vagina or throat containing dried whole or peeled rhizome or containing aqueous dispersions or aqueous extracts of whole or peeled rhizome; or | |
| (c) in dermal preparations. |
| 41324M. | Raltegravir. |
| 41355V. | Rotigotine. |
| 41469M. | Temsirolimus. |
| 5087. | 2,4-D in preparations containing 20% or less of 2,4-D. |
| 5090. | Deltamethrin – |
| (a) in aqueous preparations containing 5% or less of deltamethrin when no organic solvent other than a glycol is present; or | |
| (b) in wettable granular preparations containing 25% or less of deltamethrin when packed in child-resistant packaging each containing 3g or less of the formulation; or | |
| (c) in water-dispersible tablets each containing 500mg or less of deltamethrin in child-resistant packaging; or | |
| (d) in other preparations containing 0.5% or less of deltamethrin. |
| 6001. | Abamectin – |
| (a) in preparations for pesticidal use containing 2% or less of abamectin, except when included in Schedule 5 ; or | |
| (b) in slow-release plastic matrix ear tags for livestock use containing 1g or less of abamectin. |
| 6070. | Carbendazim except in paints, jointing compounds and sealants containing 0.5% or less of carbendazim. |
| 6103. | Coumaphos – |
| (a) in slow-release plastic matrix ear tags for livestock use containing 6g or less of coumaphos; or | |
| (b) in other preparations containing 5% or less of coumaphos. |
| 6115M. | 2,4-D except when included in Schedule 5 . |
| 6211. | Glycolic acid (including its salts and esters) in cosmetic products or when packed and labelled for use as an agricultural chemical except – |
| (a) in cosmetic preparations for salon use only which are labelled in accordance with the | |
| (b) in preparations containing 5% or less of glycolic acid; or | |
| (c) in preparations containing 20% or less of glycolic acid with a pH of 3.5 or greater. |
| 6263. | Methomyl in fly-baits containing 1% or less of methomyl and not less than 0.002% of denatonium benzoate as a bittering agent. |
| 6268M. | Methylnorbornylpyridine. |
| 6298. | Octhilinone except in paints, jointing compounds and sealants containing 1% or less of octhilinone calculated on the non-volatile content. |
| 6376. | Spirotetramat. |
| 7063M. | Cyanogen. |
| 7513M. | 1,4-butanediol (excluding its derivatives) in non-polymerised form in preparations for domestic use. |
| 7523M. | Diethylene glycol for use in toothpastes or mouthwashes, except in preparations containing 0.25% or less of diethylene glycol. |
Displayed and numbered in accordance with the
Notified in the
This order is administered in the Department of Health and Human Services.
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