Label: EQUATE ANTIBACTERIAL WIPES FRESH- benzalkonium chloride cloth

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 11, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • 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

    Fresh LabelFresh Film

  • INGREDIENTS AND APPEARANCE
    EQUATE ANTIBACTERIAL WIPES FRESH 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-287
    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
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-287-2424 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!