NDC 74955-026 Breeze Antibacterial Handsoap Berry Mixture
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What is NDC 74955-026?
What are the uses for Breeze Antibacterial Handsoap Berry Mixture?
Which are Breeze Antibacterial Handsoap Berry Mixture UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Breeze Antibacterial Handsoap Berry Mixture 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)
- COCO GLUCOSIDE (UNII: ICS790225B)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- LAURETH-7 (UNII: Z95S6G8201)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Breeze Antibacterial Handsoap Berry Mixture?
- RxCUI: 1439778 - benzalkonium chloride 0.2 % Medicated Liquid Soap
- RxCUI: 1439778 - benzalkonium chloride 2 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".