NDC 80994-004 Sanitizing Hand
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 80994-004?
What are the uses for Sanitizing Hand?
Which are Sanitizing Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Sanitizing Hand 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SUCROSE COCOATE (UNII: 3H18P0UK73)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CHAMOMILE (UNII: FGL3685T2X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
What is the NDC to RxNorm Crosswalk for Sanitizing Hand?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid 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".