NDC 72900-882 Sa Oil Free Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72900 - Essay Cosmetics Group Llc
- 72900-882 - Sa Oil Free Cream
Product Packages
NDC Code 72900-882-70
Package Description: .5 g in 1 BOTTLE, PUMP
Product Details
What is NDC 72900-882?
What are the uses for Sa Oil Free Cream?
Which are Sa Oil Free Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Sa Oil Free Cream Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- PEG-100 STEARATE (UNII: YD01N1999R)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ALLANTOIN (UNII: 344S277G0Z)
- .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
- 1,2-PROPANEDIOL, 1-BENZOATE (UNII: K4K90ZQ89N)
- .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PROPANEDIOL (UNII: 5965N8W85T)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
What is the NDC to RxNorm Crosswalk for Sa Oil Free Cream?
- RxCUI: 417424 - salicylic acid 1 % Topical Cream
- RxCUI: 417424 - salicylic acid 10 MG/ML Topical Cream
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".