Therapeutic Goods Order No. 80 - Child-Resistant Packaging Requirements for Medicines (27/08/2008)
6Application
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6 Application
(1) This Order applies to each medicine for human use that is supplied by a sponsor and that is:
(a) a registered medicine that contains a substance, or a salt, ester or other derivative of a substance, that belongs to a class of substance specified in Part 1 of Schedule 1; or
(b) a listed or registered medicine that contains a substance, or a salt, ester or other derivative of a substance, specified in Part 2 of Schedule 1 in the strength or pack size specified in Part 2 to Schedule 1; or
(c) any other medicine that is labelled or packaged in a way that states or implies to a consumer or purchaser that the product, as presented, is child‑resistant.
(2) However, this Order does not apply to a medicine that is exempted under section 7 or in relation to which an exemption from compliance with this Order has been granted by the Secretary in accordance with section 14 and 14A of the Act.