(1) For paragraph 21(a) of the Code, the following particulars are prescribed:
(a) the appropriate signal words required by the current Poisons Standard;
(b) the name of the chemical product that is to appear on a label for containers of the chemical product;
(c) the name of each active constituent of the product;
(d) the proportion of each active constituent of the product;
(e) the name of each constituent for the product that is:
(i) not an active constituent; and
(ii) classified as a poison in the current Poisons Standard;
(f) the proportion of each constituent referred to in paragraph (e);
(h) the net contents of the product;
(j) particulars determined by the APVMA CEO under subregulation (2).
(2) For paragraph 6(2)(c) of the Act, the APVMA CEO may determine additional particulars to be placed on a label for a product.
(3) For subparagraph 21(c)(iva) of the Code, the following information is prescribed in relation to the approval of a label for a chemical product, unless the information has already been recorded for the approval of the label as part of the registration of the chemical product:
(a) identifying information for the holder of the approval;
(b) identifying information for any nominated agent for the approval;
(c) the distinguishing name of the chemical product that is prescribed under paragraph 16(a) and entered in the Register;
(d) the distinguishing number of the chemical product that is entered in the Register.