NDC 68828-096 Foaming Cleanser Jafra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68828 - Jafra Cosmetics International
- 68828-096 - Foaming Cleanser
Product Packages
NDC Code 68828-096-01
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 150 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 68828-096?
What are the uses for Foaming Cleanser Jafra?
Which are Foaming Cleanser Jafra 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 Foaming Cleanser Jafra 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:
- SULISOBENZONE (UNII: 1W6L629B4K)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- SODIUM LAUROYL OAT AMINO ACIDS (UNII: FSW2K9B9N5)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Foaming Cleanser Jafra?
- RxCUI: 865105 - salicylic acid 0.5 % Medicated Liquid Soap
- RxCUI: 865105 - salicylic acid 5 MG/ML Medicated Liquid Soap
- RxCUI: 865105 - salicylic acid 0.5 % Foaming Cleanser
- RxCUI: 865105 - salicylic acid 0.5 % Mask
- RxCUI: 865105 - salicylic acid 0.5 % Topical Gel Cleanser
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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".