Food and Drug Regulations

C.01.031.2 (1) Sections C.01.029 to C.01.031 do not apply to a drug that is

• (a) a prescription drug or a drug that is required to be sold under a prescription by Part G, the Benzodiazepines and Other Targeted Substances Regulations or the Narcotic Control Regulations;

• (b) intended for parenteral use only;

• (c) in effervescent or powder form;

• (d) in suppository form;

• (e) intended for topical use, unless it is a liquid preparation containing more than five per cent alkyl salicylates;

• (f) packaged in a non-reclosable package containing not more than two adult standard dosage units per package; or

• (g) in toothpaste form.

(2) Sections C.01.029 to C.01.031 do not apply to a drug that is repackaged by a pharmacist or practitioner at the time of sale.

(3) Section C.01.031 does not apply to a drug that is

• (a) sold only in containers that have roll-on or spray applicators or permanently installed wick applicators;

• (b) sold for exclusive use in animals other than household pets; or

• (c) intended solely for use in dentists’ offices, or packaged for hospital use only.