重新应用的时间:FDA防晒霜法规的回顾及其需要更新的原因

E. Davidson
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引用次数: 0

摘要

防晒霜是预防黑色素瘤的主要产品,国外在配方和应用方面的创新为消费者提供了防晒的方法。然而,FDA旨在保护美国消费者免受无效防晒霜侵害的规定,往往成为这些创新的外国防晒霜进入美国消费者市场的障碍。本说明将解决消费者保护和促进产品创新之间的平衡问题。该说明概述了美国防晒霜监管的历史。然后讨论了目前的监管框架和美国消费者目前可以使用的防晒霜过滤器,然后提供了国外防晒霜配方创新的例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time for Reapplication: A Review of FDA Sunscreen Regulation & Why it Needs an Update
Sunscreen is a staple in melanoma prevention and foreign innovation in formulation and application provide consumers with methods of sun protection. Nevertheless, FDA regulations designed to protect American consumers from ineffective sunscreens often act as a barrier to entry for these innovative, foreign sunscreens from reaching American consumers. This Note will address balancing concerns between consumer protection and promoting product innovation. The Note outlines the history of sunscreen regulation in the United States. Then it discusses the current regulatory framework and what sunscreen filters are currently available to American consumers before providing examples of foreign innovation in sunscreen formulation.
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