Food and Drug Regulations
(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
- SOR/86-93, s. 2
- SOR/87-484, s. 4
- SOR/88-323, s. 5(F)
- SOR/93-468, s. 3
- SOR/2013-122, s. 8
- Date modified: