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This bill amends the Federal Food, Drug, and Cosmetic Act to establish a distinct regulatory pathway for homeopathic drug products. It defines homeopathic drugs and ingredients, exempts them from most FDA approval requirements that apply to conventional drugs, and instead requires compliance with standards from the Homeopathic Pharmacopoeia of the United States or accredited voluntary consensus standards. The bill imposes safety and quality requirements, labeling standards for retail products, and creates a Homeopathic Drug Product Advisory Committee to review manufacturer petitions for exemptions or alternative standards.
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