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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  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Use

    • Decreases bacteria on skin
  • Warnings

    For external use only

    Keep out of eyes. In case of eye contact, rinse with water.

    If irritation develops, discontinue use.

    Consult a doctor if irritation persists more than 72 hours.

    If swallowed, seek medical attention or contact a Poison Control Center.

    Keep out of the children, except with adult supervision.

  • Directions for use

    Thoroughly wipe hands and face as desired.

    Allow to dry without wiping.

    Discard wipe in trash receptacle after use. Do not flush.

  • Inactive ingredients

    Aqua, Phenoxyethanol, Perfume, Propylene Glycol, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Benzoic acid, Tetrasodium Edta, Dehydroacetic acid, Glycerin, Polysorbate 20, Citric acid

  • SPL UNCLASSIFIED SECTION

    KILLS 99.99% OF GERMS

    Distributed by Alta Sales Inc.

    S. Hackensack NJ, 07606

    www.altawipes.com

    info@altawipes.com

    Made in Turkey

  • Packaging

    IMAGEIMAGE

  • INGREDIENTS AND APPEARANCE
    ALTA ANTIBACTERIAL HAND WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79165-777
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79165-777-2020 in 1 PACKET07/01/2020
    13.6 g in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:79165-777-9090 in 1 PACKET07/01/2020
    23.6 g in 1 PACKAGE; Type 0: Not a Combination Product
    3NDC:79165-777-8080 in 1 CANISTER08/06/202007/31/2023
    33.6 g in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2020
    Labeler - Alta Sales Inc (080087931)
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