Label: BENZALKONIUM CHLORIDE- sanitizing hand wipes cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 4, 2024

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  • Active ingredients

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial

  • Uses

    • Hand Sanitizer to help reduce bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only.

  • When using this product

    avoid contact with eyes. In case of contact, flush with water.

  • Stop use and ask a doctor

    If redness or irritation develops and persists for more than 72 hours

  • Keep out of reach of children

    Children should be supervised when using this product

  • Directions

    Take wipe and rub thoroughly over all surface of both hands. Wet hands thoroughly with wipes. Rub hand together briskly to dry without wiping. Dispose of wipe. Do not flush.

  • Inactive ingredients

    Purified Water, Decyl Glucoside, Aloe Barbadensis (Aloe) Leaf Extract, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Eucalyptus Globulus Oil, Mentha Piperita (Peppermint) Oil.

  • Principal Display Panel

    Lavender Rosewood + Aloe

    ALOH

    Clean Hands, Clear Mind

    Kills 99.9% of Germs*

    20 Skin-Softening Sanitizing Hand Wipes

    Do Not Peel

    Label

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE 
    sanitizing hand wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82355-552
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0013 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    ANIBA ROSAEODORA WHOLE (UNII: 5ZTZ6VF78R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82355-552-0120 in 1 PACKAGE01/04/2024
    11 mg in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00401/04/2024
    Labeler - ALO NEW YORK LLC (110122374)
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