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FDA Advances Proposed Rule on Sunscreens

机译:FDA提出了防晒霜的拟议规则

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In February,The U.S.Food & Drug Administration(FDA)issued a proposed rule that would update regulatory requirements for most sunscreen products in the U.S.The action is aimed at bringing non-prescription,over-the-counter(OTC)sunscreens that are marketed without FDA-approved applications up to date with the latest science to better ensure consumers have access to safe and effective preventative sun care options.Among its provisions,the proposal addresses sunscreen active ingredient safety,dosage forms and sun protection factor(SPF)and broad-spectrum requirements.It also proposes updates to how products are labeled to make it easier for consumers to identify key product information.“Broad spectrum sunscreens with SPF values of at least 15 are critical to the arsenal of tools for preventing skin cancer and protecting the skin from damage caused by the sun's rays,yet some of the essential requirements for these preventive tools haven't been updated in decades,” explained FDA Commissioner Scott Gottlieb,M.D.
机译:2月份,美国食品和药物管理局(FDA)发布了一项拟议规则,该规则将更新USTHE行动中的大多数防晒产品的监管要求,旨在带来销售的非处方,柜台上的柜台(OTC)防晒霜如果没有FDA批准的应用,最新的应用程序更新,以更好地确保消费者可以获得安全有效的预防阳光照顾选择。该提案解决了防晒活性成分安全性,剂型和防晒系数(SPF)和广泛-SpectRum要求。它还提出了对产品的标记方式更新,以使消费者更容易识别关键产品信息。“具有至少15个具有至少15个具有至少15个具有至关重要的广谱防晒对防止皮肤癌的工具库是至关重要的Sun的光线造成的伤害,但这些预防工具的一些基本要求尚未在几十年内更新,“FDA专员委员会解释说Cott Gottlieb,M.D。

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