Dale Wilson Brummitte, Moon Summer, Armstrong Frank
Suny at Buffalo School of Medicine and Suny at Buffalo School of Dentistry, Hamburg, New York;
J Clin Aesthet Dermatol. 2012 Sep;5(9):18-23.
In the past, manufacturers' labeling of sunscreen varied greatly, confusing the consumers regarding efficacy and the appropriate photoprotection provided by their products. Therefore, in June 2011, the United States Food and Drug Administration issued new guidelines for sunscreen labeling. Sunscreen products are over-the-counter drugs; therefore, they are regulated by the United States Food and Drug Administration to determine safety, efficacy, and labeling. This article discusses ultraviolet radiation and the positive and negative effects of ultraviolet radiation, provides a review of sunscreens, and discusses the new United States Food and Drug Administration regulations for sunscreens.
过去,防晒霜制造商的产品标签差异很大,这让消费者对产品的功效以及所提供的适当光防护感到困惑。因此,2011年6月,美国食品药品监督管理局发布了防晒霜标签的新指南。防晒产品属于非处方药物;因此,它们受美国食品药品监督管理局监管,以确定其安全性、功效和标签。本文讨论了紫外线辐射以及紫外线辐射的正负效应,对防晒霜进行了综述,并探讨了美国食品药品监督管理局关于防晒霜的新规定。