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Natural Health Products Regulations

Version of section 22 from 2021-03-31 to 2024-11-26:

  •  (1) Subject to subsection (2), the licensee shall provide the Minister with the following information prior to commencing the sale of the natural health product:

    • (a) in respect of each manufacturer, packager, labeller and importer of the natural health product

      • (i) the person’s name, address and telephone number, and if applicable, the person’s facsimile number and electronic mail address, and

      • (ii) if the person conducts the activity in Canada, the number assigned to the site licence issued in respect of that activity;

    • (b) the name, address and telephone number, and if applicable, the facsimile number and electronic mail address of each distributor of the natural health product;

    • (c) the address of each building in which the natural health product is manufactured, packaged or labelled;

    • (d) the address of each building in which the natural health product is stored for the purposes of importation or distribution; and

    • (e) if the natural health product is imported, evidence establishing that the natural health product will be manufactured, packaged, labelled, imported, distributed and stored in accordance with the requirements set out in Part 3 or in accordance with requirements that are equivalent to those set out in Part 3.

  • (2) If the natural health product is one in respect of which a drug identification number is assigned in accordance with subsection C.01.014.2(1) of the Food and Drug Regulations and at the time the product licence is issued in respect of the natural health product it is already being sold, the licensee shall provide the information referred to in subsection (1) within 30 days after the day on which the product licence is issued.

  • SOR/2018-69, s. 46(F)
  • SOR/2021-46, s. 17(F)
  • SOR/2021-46, s. 19(E)

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