36Ampoules, pre‑filled syringes and injection vials

36  Ampoules, pre‑filled syringes and injection vials

 (1) The requirements of Subdivision B do not apply to a selected container of poison or an ampoule of poison (other than an ampoule to which subsection (2) applies) when:

 (a) the poison is therapeutic goods and is labelled in accordance with the standards for the goods specified in orders made under subsection 10(1) of the Act; or

 (b) the selected container or ampoule is:

 (i) packed in a primary pack labelled in accordance with Subdivision B; and

 (ii) labelled with:

 (A) the approved name of the poison and the quantity, proportion or strength of the poison in accordance with section 34; and

 (B) the name of the manufacturer or distributor or the brand name or trade name used exclusively by the manufacturer or distributor for the poison; and

 (C) if the poison is only for the treatment of animals—the cautionary statement:

  written in sans serif capital letters.

 (2) The requirements of Subdivision B do not apply to a selected container of poison that is a plastic ampoule that is continuous with a strip of the same material and opens as it is detached from the strip when:

 (a) the poison is therapeutic goods and is labelled in accordance with the standards for the goods specified in orders made under subsection 10(1) of the Act; or

 (b) the poison is not therapeutic goods and all of the following apply:

 (i) the ampoule is packed in a primary pack labelled in accordance with Subdivision B;

 (ii) the strip is labelled in accordance with this section;

 (iii) the ampoule is labelled with:

 (A) the approved name of the poison or the trade name of the poison; and

 (B) the quantity, proportion or strength of the poison in accordance with section 34.