Published in the Commonwealth of Australia Gazette No. GN 32, 13 August 2003
Therapeutic Goods Act 1989
I, TERRY SLATER, National Manager, Therapeutic Goods Administration, delegate of the Parliamentary Secretary to the Minister for Health and Ageing, under subsection 17 (5) of the Therapeutic Goods Act 1989, require the following therapeutic goods to be included in the part of the Australian Register of Therapeutic Goods for listed goods:
preparations, referred to in item 3 of Schedule 4, Part 1 of the Therapeutic Goods Regulations (the Regulations) that contain, as an ingredient, cold-pressed neem (Azadirachta indica) seed oil for topical application at concentrations up to 1%, and at concentrations greater than 1% when in a container fitted with a child resistant closure and labelled with the statements:
"Not to be taken";
"Keep out of reach of children"; and
"Do not use if pregnant or likely to become pregnant."
which is to be mentioned in Division 2 of Part 4 of Schedule 4 of the Regulations; and
preparations, referred to in item 3 of Schedule 4, Part 1 of the Regulations that contain, as an ingredient, calcium sodium caseinate, and that are supplied with a label that includes a statement to the effect "contains cow's milk protein", which is to be mentioned in Division 3 of Part 5 of Schedule 4 of the Regulations.
Dated 4 August 2003
National Manager, Therapeutic Goods Administration Delegate of the Parliamentary Secretary
The Department of Health and Aged Care acknowledges First Nations peoples as the Traditional Owners of Country throughout Australia, and their continuing connection to land, sea and community. We pay our respects to them and their cultures, and to all Elders both past and present.