Label: ALTA ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 79165-777-20, 79165-777-80, 79165-777-90 - Packager: Alta Sales Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 20, 2026
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- Drug Facts
- Active Ingredient
- Purpose
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- Inactive ingredients
- SPL UNCLASSIFIED SECTION
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INGREDIENTS AND APPEARANCE
ALTA ANTIBACTERIAL HAND WIPES
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79165-777 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) BENZOIC ACID (UNII: 8SKN0B0MIM) EDETATE SODIUM (UNII: MP1J8420LU) DEHYDROACETIC ACID (UNII: 2KAG279R6R) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79165-777-20 20 in 1 PACKET 07/01/2020 1 3.6 g in 1 PACKAGE; Type 0: Not a Combination Product 2 NDC:79165-777-90 90 in 1 PACKET 07/01/2020 2 3.6 g in 1 PACKAGE; Type 0: Not a Combination Product 3 NDC:79165-777-80 80 in 1 CANISTER 08/06/2020 07/31/2023 3 3.6 g in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 07/01/2020 Labeler - Alta Sales Inc (080087931)

