化妆品和药品在美国的法律区别

P. Hutt
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引用次数: 5

摘要

《联邦食品、药品和化妆品法案》(FD&C法案)在美国对化妆品和药品制定了截然不同的监管要求。本章追溯了美国对这两类产品的监管政策的历史,讨论了美国法律对同时属于这两类产品(即美容药物)的应用,并考虑了解决长期存在的担忧的潜在策略,即该法案的药物条款对美容药物施加了过于严格的要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The legal distinction in the United States between a cosmetic and a drug
The Federal Food, Drug, and Cosmetic Act (FD&C Act) establishes substantially different regulatory requirements in the United States for cosmetics and drugs. This chapter traces the history of U.S. regulatory policy for these two categories of products, discusses the application of U.S. law to products that fall within both categories at the same time (i.e., cosmetic drugs), and considers potential strategies for resolving the long-standing concern that the drug provisions of the Act impose overly stringent requirements on cosmetic drugs.
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