Label: BENZALKONIUM CHLORIDE- dual action antibacterial wipes cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 29, 2022

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  • Active ingredient

    Antimicrobial

  • Purpose

    Antimicrobial

  • Uses

    • to sanitize hands without requiring water or a rinse
    • kills 99.9% of most common germs*
  • Warnings

    For external use only

    When using this product

    • do not use in or near eyes
    • discontinue use if irritation and redness develop

    Keep out of reach of children

    In case of accidental ingestion, seek medical attention or contact a posion control center immediately.

  • Directions

    • wet hands thoroughly with wipe
    • allow to dry without rinsing
  • Other information

    store at room temperature 15° to 25° C (59° -77°F)

  • Inactive ingredients

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

  • Principal Display Panel

    dual action

    antibacterial wipes

    Moisturizing Formula

    Non-Alcohol Based

    Gently Cleans and Refreshes

    *Kills 99.99% of germs

    that may cause illness,

    including E. Coli and MRSA

    in just 15 seconds

    2000 Pre-Moistened

    Wipes

    8" x 5"

    wipes

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE 
    dual action antibacterial wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73062-400
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73062-400-012000 in 1 CONTAINER; Type 0: Not a Combination Product10/26/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/26/2021
    Labeler - Avro Enterprises LLC (804030166)
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