Label: ALTA ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth
- NDC Code(s): 79165-777-20, 79165-777-80, 79165-777-90
- Packager: Alta Sales Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 19, 2023
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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 not final part333A 07/01/2020 Labeler - Alta Sales Inc (080087931)