Food and Drug Regulations

J.01.032 Every package that contains a restricted drug shall be labelled so that the inner and outer labels thereon show

• (a) the proper name or, if there is no proper name, the common name of the drug;

• (b) the net contents of the package;

• (c) the unit strength of the drug where it is in unit form;

• (d) the lot number of the drug;

• (e) the words “Restricted Drug”; and

• (f) the name and address of the producer, maker or assembler of the drug.