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The shellac coating is insoluble in stomach acid and may make the tablet difficult for the body to break down or assimilate. For this reason, it can also be used as an ingredient in time-released, sustained or delayed-action pills. The product is listed on the U.S. Food and Drug Administration's (FDA) inactive ingredient list. [7]
An ingredient with a GRAS designation is exempted from the usual Federal Food, Drug, and Cosmetic Act (FFDCA) food additive tolerance requirements. [2] The concept of food additives being "generally recognized as safe" was first described in the Food Additives Amendment of 1958 , and all additives introduced after this time had to be evaluated ...
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The U.S. Food and Drug Administration (FDA) has approved this chemical for many uses, [24] and it is generally recognized as safe . PVP is included in the Inactive Ingredient Database for use in oral, topical, and injectable formulations.
The U.S. Food and Drug Administration (FDA) announced that it plans to ban products containing phenylephrine, an ingredient found in many over-the-counter (OTC) oral cold and flu medications.
The Consumer Health Product Database is a web-based application that allows the public to search for specific products or specific chemical ingredients. It is a collection of publicly available information, mostly from product labels and Safety Data Sheets (former MSDS) provided by the product's manufacturer. [ 1 ]
Unique Ingredient Identifier; Proprietary database identifiers include those assigned by First Databank, Micromedex, MediSpan, Gold Standard Drug Database (published by Elsevier), and Cerner Multum MediSource Lexicon; these are cross-indexed by RxNorm, which also assigns a unique identifier (RxCUI) to every combination of active ingredient and ...
Sodium tallowate is a common soap ingredient derived from tallow—the fat of animals such as cattle and sheep. [31] A popular alternative to this ingredient is sodium palmate, which is derived from palm oil. [32] Soap is a pharmaceutical according to the United States Food and Drug Administration. [33]