NDC 78939-001 Antibacterial Hand
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 78939-001?
What are the uses for Antibacterial Hand?
Which are Antibacterial 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 Antibacterial 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)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CITRAL (UNII: T7EU0O9VPP)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- GERANIOL (UNII: L837108USY)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- LAURETH-10 (UNII: BD7AST04GA)
What is the NDC to RxNorm Crosswalk for Antibacterial 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".