Label: BENZALKONIUM CHLORIDE- antibacterial hand wipes cloth

  • NDC Code(s): 78691-140-04, 78691-140-06
  • Packager: Quest USA Corp
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 1, 2024

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  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    • Hand sanitizer to help reduce bacteria
    • For use when soap and water are not available
  • Warnings

    For external use only.

    Do not use

    • in children less than 2 months old.
    • on open skin wounds.

    When using this product

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor

    if irritation or rash occurs. These may be signs of serious condition.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply to hands, allow to air dry without wiping.
    • Children under 6 years of age should be supervised when using this product.
  • Other information

    • Store in a cool, dry place, between 15°-30°C (59°F-86°F).
    • Avoid freezing and excessive heat above 40°C (104°F).
  • Inactive ingredients

    Aloe Barbadensis Leaf Extract, Citric Acid, Decyl Glucoside, Disodium EDTA, Fragrance, Phenoxyethanol, Potassium Sorbate, Purified Water, Sodium Benzoate

  • Questions?

    call 718-975-2586

  • PRINCIPAL DISPLAY PANEL

    1600fr

    1600Ba

  • PRINCIPAL DISPLAY PANEL

    1400New

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE 
    antibacterial hand wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78691-140
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78691-140-041400 in 1 CONTAINER; Type 0: Not a Combination Product03/04/2022
    2NDC:78691-140-061600 in 1 CONTAINER; Type 0: Not a Combination Product03/04/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/04/2022
    Labeler - Quest USA Corp (079869689)
    Registrant - Quest USA Corp (079869689)
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