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Rulemaking History of General Labeling Requirements for OTC Drug ProductsView by Date
OTC Drug Product Labeling Regulations (21 CFR part 201 subpart C): Labeling Requirements for Over-the-Counter Drugs
OTC Drug Product Labeling found on this page:
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Draft Guidance
Guidance
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Date created: December 28, 2006; Last updated January 9, 2009
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