Label: WALGREENS ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth

  • NDC Code(s): 0363-5189-01, 0363-5189-02
  • Packager: Walgreen Co.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 21, 2024

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.11%

  • Purpose

    Antibacterial

  • Uses

    Decreases bacteria on skin

  • Warnings

    For external use only

    Do not use

    •If you are allergic to any of the ingredients

    When using this product •Do not get into eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor •If irritation or rash develops and continues for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    •Adults and children 2 years and older: 

       Wipe hands thorough with product and allow to dry without wiping.

    •Children under 2 years of age: Consult a doctor before use.

  • Inactive ingredients

    Water, Alcohol, Propylene Glycol, Phenoxyethanol, Lauryl Glucoside, Tetrasodium EDTA, 2-Bromo-2-Nitropropane-1,3-Diol, Citric Acid, Fragrance, Iodopropynyl Butylcarbamate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract.

  • SPL UNCLASSIFIED SECTION

    Gentle cleansing

    Kills 99.9% of germs

    Hypoallergenic

    DO NOT FLUSH

    DISTRIBUTED BY: WALGREEN CO.

    DEERFIELD, IL 60015

    100% SATISFACTION GUARANTEED

    walgreens.com  1-877-274-8358

    ©2024 Walgreen Co.  MADE IN CHINA

  • Packaging

    Walgreens Antibacterial Hand Wipes

  • INGREDIENTS AND APPEARANCE
    WALGREENS ANTIBACTERIAL HAND WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5189
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.11 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    BRONOPOL (UNII: 6PU1E16C9W)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMOMILE (UNII: FGL3685T2X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-5189-0175 in 1 POUCH05/21/2024
    13.83 mL in 1 PATCH; Type 0: Not a Combination Product
    2NDC:0363-5189-0220 in 1 POUCH05/21/2024
    23.83 mL in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/21/2024
    Labeler - Walgreen Co. (008965063)
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