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In the U.S., under the Food, Drug, and Cosmetic Act and the Fair Packaging and Labeling Act, certain accurate information is a requirement to appear on labels of cosmetic products. [6] In Canada, the regulatory guideline is the Cosmetic Regulations. [7] Ingredient names must comply by law with EU requirements by using INCI names. [8]
It is one of 26 published standards that are devoted to the cosmetic industry sector. [1] ISO 22715 does not regulate what products are to be considered cosmetic. This determination is left to the national regulations of those countries that follow the ISO 22715 and use it as a guide to best practices for packaging and labeling cosmetic ...
Although the FDA does not have the resources to inspect all cosmetic products on the market, it can issue penalties for various violations involving packaging and labeling. It is the manufacturer's responsibility to make sure that its product is safe for public consumption.
The FDA, which regulates the US cosmetic industry, says "FDA has not defined the term “natural” and has not established a regulatory definition for this term in cosmetic labeling." [33] It goes on to warn consumers, "choosing ingredients from sources you consider “organic” or “natural” is no guarantee that they are safe."
Current good manufacturing practices (cGMP) are those conforming to the guidelines recommended by relevant agencies.Those agencies control the authorization and licensing of the manufacture and sale of food and beverages, [1] cosmetics, [2] pharmaceutical products, [3] dietary supplements, [4] and medical devices. [5]
Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.
The Fair Packaging and Labeling Act required all "consumer commodities" to have a label. Under the act, consumer commodities were defined as any food, drug, device, or cosmetic, that is produced or distributed for sale through retails sales/agencies for consumption by individuals or used by individuals for the purpose of personal care.
Structured Product Labeling (SPL) is a Health Level Seven International (HL7) standard which defines the content of human prescription drug labeling in an XML format. [1] The "drug labeling" includes all published material accompanying a drug, such as the Prescribing Information which contains a great deal of detailed information about the drug.