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110170. ARTICLE 4. Export Documents .... distributor. 109910. Department means the State Department of Health Services. ..... (commencing with Section 11340) of Part 1 of Division 3 of Title 2 of
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The Sherman Food, Drug, and Cosmetic Act is a comprehensive federal law that regulates food safety, drugs, and cosmetics in the United States. It ensures that these products are safe for consumption and properly labeled.
Manufacturers, distributors, and sellers of food, drugs, and cosmetics are required to comply with the Sherman Food, Drug, and Cosmetic Act. This includes businesses involved in the production and marketing of these products.
To fill out compliance documentation related to the Sherman Food, Drug, and Cosmetic Act, entities must provide specific information about their products, including ingredients, labeling, manufacturing practices, and safety data, typically as outlined in regulatory guidelines.
The purpose of the Sherman Food, Drug, and Cosmetic Act is to protect public health by ensuring the safety, efficacy, and security of food, drugs, and cosmetics through regulation and enforcement.
Information that must be reported includes product ingredients, nutritional data, safety evidence, manufacturing processes, and labeling claims, all of which are essential for regulatory compliance and consumer safety.
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