Language selection

Government of Canada

Search

Natural Health Products Regulations (SOR/2003-196)

Regulations are current to 2026-09-30 and last amended on 2025-06-21. Previous Versions

  •  (1) If a practitioner or pharmacist has signed an order specifying the proper name or common name, the brand name and the quantity of a natural health product, the person who receives the order may distribute or cause to be distributed the natural health product, in dosage form, as a sample to that practitioner or pharmacist if the natural health product meets the requirements of these Regulations.

  • (2) An order referred to in subsection (1) may provide that the order be repeated at specified intervals during any period that does not exceed six months.

  • (3) Despite subsection (1), a person may distribute or cause to be distributed a natural health product, in dosage form, as a sample to a practitioner or pharmacist without a signed order if that natural health product has a localized effect and is for administration either in the oral cavity or on the skin, or is a throat lozenge, and if all of the following conditions are met:

    • (a) the natural health product is part of a class of natural health products that is set out in column 1 of List A and contains, as its only medicinal ingredients, one or more of those set out in column 2, each of which corresponds to that class, in the corresponding quantity set out in column 3, and the natural health product is consistent with the descriptive information set out in columns 4 to 6;

    • (b) the expiry date of the natural health product falls on a day that is

      • (i) at least 30 days after the day on which it is distributed, if the expiry date consists of a day, month and year, or

      • (ii) in a month that follows the month in which it is distributed, if the expiry date consists only of a month and year;

    • (c) the natural health product meets the requirements of these Regulations.

  • (4) For the purposes of this section, practitioner and pharmacist have the same meaning as in subsection C.01.001(1) of the Food and Drug Regulations.

Page Details

Date modified: