Label: EQUATE ANTIBACTERIAL WIPES CITRUS- benzalkonium chloride cloth

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

Drug Label Information

Updated December 11, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.115%

  • Purpose

    Antibacterial

  • Uses

    For handwashing to decrease bacteria on the skin

  • Warnings

    For external use only

  • Do not use

    • In the eyes
    • If you are allergic to any of the ingredients
  • When using this product

    if eye contact occurs, rinse eyes thoroughly with water.

  • Stop use and ask a doctor

    If irritation and redness develops and persist for more than 72 hours.

  • Keep out of reach of children

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

  • Directions

    • Storage, Store at room temperature
    • Use. Apply wipe thoroughly to hands as desired. Allow to dry without wiping.
  • Inactive ingredients

    Water, Caprylyl Glycol, Sodium Benzoate, Polysorbate 20, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Citric Acid, Fragrance

  • Package Label

    FilmLabel

  • INGREDIENTS AND APPEARANCE
    EQUATE ANTIBACTERIAL WIPES CITRUS 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-371
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.115 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-371-2424 in 1 PACKAGE; Type 0: Not a Combination Product11/29/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00311/29/2024
    Labeler - Walmart, Inc. (051957769)
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