Label: EQUATE ANTIBACTERIAL FRESH HAND WIPES- benzalkonium chloride cloth

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

Drug Label Information

Updated December 11, 2024

If you are a consumer or patient please visit this version.

  • 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

    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
    • Dispensing Remove lid and throat seal. Replace lid and lift tab at front of lid. Pull up corner of center sheet and thread through dispenser slit in lid. Close lid to retain moisture.
    • Use. Apply wipe thoroughly to hands as desired. Allow to dry without wiping.
    • Disposal. Dispose of used wipes in a trash receptacle after use. Do not flush.
  • Inactive ingredients

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

  • Package Label

    Fresh 40 Ct Front LabelFresh 40 Ct Back Label

  • INGREDIENTS AND APPEARANCE
    EQUATE ANTIBACTERIAL FRESH HAND WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-110
    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:79903-110-4040 in 1 CANISTER; Type 0: Not a Combination Product04/28/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/28/2024
    Labeler - Walmart, Inc. (051957769)