NDC 76279-420 Softone Luxury Foam Antibacterial Skin Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76279-420?
What are the uses for Softone Luxury Foam Antibacterial Skin Cleanser?
Which are Softone Luxury Foam Antibacterial Skin Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Softone Luxury Foam Antibacterial Skin Cleanser 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM CUMENESULFONATE (UNII: 5798KA13PG)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Softone Luxury Foam Antibacterial Skin Cleanser?
- RxCUI: 413247 - triclosan 0.5 % Medicated Liquid Soap
- RxCUI: 413247 - triclosan 5 MG/ML Medicated Liquid Soap
- RxCUI: 413247 - triclosan 0.5 % Foaming Medicated Hand Soap
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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".