Food and Drug Regulations

C.03.207 Every component shall be labelled to show

• (a) adequate identification of the component and an adequate description of its function;

• (b) where applicable, a quantitative list of its ingredients or a reference to the label of the kit that shows such information;

• (c) the name of the distributor referred to in paragraph C.01A.003(b);

• (d) the lot number;

• (e) a statement of any special storage requirements with respect to temperature and light;

• (f) the date after which the component is not recommended for use, the name of the month being written in full or designated by letter abbreviation; and

• (g) adequate directions for use or a reference to the accompanying package insert that shows such directions.