NDC 81608-003 Saloon Antibacterial Hand Wash Ocean
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 81608-003?
What are the uses for Saloon Antibacterial Hand Wash Ocean?
Which are Saloon Antibacterial Hand Wash Ocean UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Saloon Antibacterial Hand Wash Ocean 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)
- COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
- LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
- MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- COCAMINE OXIDE (UNII: QWA2IZI6FI)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- MALIC ACID (UNII: 817L1N4CKP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
What is the NDC to RxNorm Crosswalk for Saloon Antibacterial Hand Wash Ocean?
- 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".