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Guidance for Industry Labeling OTC Human Drug Products Questions and Answers. S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDR)
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What is fda?
FDA stands for Food and Drug Administration. It is a regulatory agency responsible for protecting the public health by ensuring the safety and efficacy of food, drugs, medical devices, and other products.
Who is required to file fda?
Manufacturers, distributors, and importers of food, drugs, and medical devices are typically required to file with the FDA.
How to fill out fda?
To fill out an FDA form, you typically need to provide information about the product being marketed, its ingredients, manufacturing process, intended use, and any known risks.
What is the purpose of fda?
The purpose of the FDA is to protect and promote public health by regulating the safety, efficacy, and labeling of food, drugs, and medical devices.
What information must be reported on fda?
Information required on FDA forms may include product labeling, manufacturing processes, ingredients, intended use, and any known risks or side effects.
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