NDC 78089-047 Alps Ultraclean Antibacterial Wet Wipes
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What is NDC 78089-047?
What are the uses for Alps Ultraclean Antibacterial Wet Wipes?
Which are Alps Ultraclean Antibacterial Wet Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Alps Ultraclean Antibacterial Wet Wipes 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)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- LIME OIL (UNII: UZH29XGA8G)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- CITRAL (UNII: T7EU0O9VPP)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- BENZYL BENZOATE (UNII: N863NB338G)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
What is the NDC to RxNorm Crosswalk for Alps Ultraclean Antibacterial Wet Wipes?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
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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".