Natural Health Products Regulations (SOR/2003-196)

14 (1) A product licence shall set out the following information:

• (a) the name and address of the licensee;

• (b) the product number of the natural health product;

• (c) the dosage form that is authorized for the natural health product;

• (d) the recommended route of administration that is authorized for the natural health product;

• (e) the recommended dose that is authorized for the natural health product;

• (f) the recommended duration of use, if any, that is authorized for the natural health product;

• (g) in respect of each medicinal ingredient of the natural health product

  • (i) its authorized quantity per dosage unit,

  • (ii) its authorized potency, if any, and

  • (iii) its authorized source material;

• (h) the recommended use or purpose that is authorized for the natural health product; and

• (i) the date on which the licence was issued.

(2) Within 60 days after the day on which the product licence is issued, the licensee shall notify the Minister of any information set out on the licence that the licensee knows to be incorrect.