Cosmetic Good Manu factu ring Practice (GMP) Gu idelines/Inspection Checklist 美国化妆品良好生产规范指南 1 美國化妆品良好生产规范指南 February 12, 1997; Updated April 24, 2008 The Federal Food, Drug and Cosmetic Act1 prohibits the introduction or delivery for introduction into interstate commerce of cosmetics that are adulterated or misbranded (Sec. 301). 联邦食品，药品和化妆品法案（The Federal Food, Drug and Cosmetic Act, 以下简称FD&C 法案）禁止在州际直接贸易的化妆品是掺杂的或贴假标签的情况。(Sec. 301) A cosmetic may be deemed adulterated (Sec. 601) for essentially four reasons, namely: 以下4 种情况下，化妆品被认为是可能掺杂的。(Sec. 601) 1. It may be injurious to users under conditions of customary use because it contains, or its container is composed of, a potentially harmful substance. 客户在使用过程中，由于化妆品本身含有或在包装容器中有潜在的，对人体有害的成份而使用户受到伤害的。 2. It contains filth. 本身含有不洁成份的。 3. It contains a non-permitted, or in some instances non-certified, color additive. 本身含有禁用成份，例如：未认可的色素添加剂。 4. It is manufactured or held under insanitary conditions whereby it may have become injurious to users or contaminated with filth. 在不卫生条件下生产的，或保留的，可导致产品伤害用户有害或被不洁成份所污染。 A cosmetic may be deemed misbranded (Sec. 602) for reasons of: 以下几种情况下，化妆品被认为可能会认为贴假标签。(Sec. 602) 1. False or misleading labeling. 虚假的标签或存在误导信息的标签。 Cosmetic Good Manu factu ring Practice (GMP) Gu idelines/Inspection Checklist 美国化妆品良好生产规范指南 2 2. Failure to state prominently and conspicuously any information required by or under authority of this act. 显着违反了联邦食品，药品和化妆品法案的要求在标签上声明的信息要求。 3. Misleading container presentation or fill. 在容器上...
