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Guideline for Selling Sunscreen Products in the US In June 2011, the U.S. Food and Drug Administration (FDA) announced new requirements for the labeling of overthecounter (OTC) sunscreen products.
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Questions and Answers FDA is a process where manufacturers and distributors of FDA-regulated products provide responses to inquiries from the Food and Drug Administration (FDA) regarding their products.
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To fill out questions and answers FDA, companies must respond to inquiries from the FDA in a timely and accurate manner.
The purpose of questions and answers FDA is to ensure the safety and effectiveness of FDA-regulated products by addressing any concerns or inquiries from the FDA.
Companies must report any relevant information about their products, including safety data, labeling information, and manufacturing processes, in questions and answers FDA.
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