NDC 11673-808 Foaming Hand Wash
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 11673-808?
What are the uses for Foaming Hand Wash?
Which are Foaming Hand Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Foaming Hand Wash 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Foaming Hand Wash?
- RxCUI: 1053855 - triclosan 0.46 % Medicated Liquid Soap
- RxCUI: 1053855 - triclosan 4.6 MG/ML Medicated Liquid Soap
- RxCUI: 1053855 - triclosan 0.46 % Foaming Medicated Hand Soap
* Please review the disclaimer below.
[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".