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This labelling standard describes the requirements necessary to receive marketing authorization (Drug identification number (DIN)) for oral expectorant nonprescription product …
This policy outlines Health Canada's current approach with respect to compounding of NHPs. The NHP Compounding Policy distinguishes between the …
The Natural Health Products Regulations (NHP Regulations) do not specify whether raw materials are or are not included in the …
This labelling standard describes the requirements necessary to receive market authorization (a Drug Identification Number (DIN)) for non-prescription oral antitussive …
To help facilitate the free-flow of natural health products across Canada's borders, Health Canada has established several Mutual Recognition Agreements …
Natural toxins are chemicals that are naturally produced by living organisms. These toxins are not harmful to the organisms themselves …
When you buy non-prescription (over-the-counter) medications for you and your family, you need information to help you make an informed …
The Government of Canada is committed to oversight for natural health products that protects consumers' health and safety while enabling …
A non-prescription drug Category IV Monograph outlines the permissible conditions of use and labelling requirements, such as dose, intended use, …
Labelling standards are developed for drugs that have a well characterized safety and efficacy profile under specific conditions of use. …