Non-prescription Drugs: Labelling Standards - Drug Product (French, HTML)

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HTML

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Publisher-reported update

2021-07-07

A nonprescription drug labelling standard outlines the permissible conditions of use and labelling requirements, such as dose, intended use, directions for use, warnings, active ingredients and combinations thereof. Labelling standards are developed for drugs that have a well characterized safety and efficacy profile under specific conditions of use.

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