Label: HAND WIPES- benzalkonium chloride swab

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 16, 2024

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  • Active ingredient

    Benzalkonium chloride.........0.13%

  • Purpose

    Antimicrobial

  • Uses

    • For hand sanitizing to decrease bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only

    ​Do not use if you are allergic to any of these ingredients

    When using this product

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

    Stop use and ask a doctor

    If irritation or redness develops, or if condition persists for more than 72 hours.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222)

  • Directions

    • adults and childrens 2 years and over: apply to hands, allow to dry without wiping
    • children under 2 years: ask a doctor before use   
  • Other information

    • Store at room temperature
    • keep closed tightly
    • may discolor certain fabrics or surfaces
  • Inactive ingredients

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

  • Principal Display Panel

    NDC: 63940-036-36

    Compare to Purell ®​ Hand Sanitizing Wipes

    36 hand wipes

    CORE VALUES TM​antibacterial 

    Hand Wipes

    KILLS 99.9% of germs

    Clean Scent

    Perfect for Travel

    36 - Wet Hand Wipes

    5.7 in. x 7.5 in. (14.5cm x 19.1cm)

    Label

  • INGREDIENTS AND APPEARANCE
    HAND WIPES 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-036
    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)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63940-036-3636 in 1 PACKAGE05/26/2020
    10.13 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/26/2020
    Labeler - Harmon Stores Inc. (804085293)
    Establishment
    NameAddressID/FEIBusiness Operations
    Precare Corp.117111327manufacture(63940-036)
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