Label: WIPEX- antibacterial wipe cloth

  • NDC Code(s): 74680-201-63, 74680-201-91
  • Packager: Unico International Trading Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active Ingredient

    Benzalkonium chloride 0.13%

  • Keeo Out of the Reach of Children

    Keep out of the reach of children. If swallowed, get medical help or contact a Poison Contrl right away.

  • Warning

    For external use only. Avoid cntact with the eyes. If in eyes, flush thoroughly with water.

  • Inactive Ingredients

    Sodium benzoate, sodium chloride, citric acid, potassium sorbate, sodium hydroxymethylglycinate, aloe vera, water

  • Purpose

    Antiseptic

  • To disperse

    To begin: Break tab on bucket rim and pull off cover. Open bag inside to expose wipes, then thread center wipe through the lid. Replace bucket cover to maintain moisture.

  • Stop Use

    Stop and ask a doctor if:

    Irritation or redness developes.

    Conditions persists for more than 72 hours.

  • To Use

    Sanitize hands or other affected area. Discard in trash after use.

  • PRINCIPAL DISPLAY PANEL

    Wipex 400

  • INGREDIENTS AND APPEARANCE
    WIPEX 
    antibacterial wipe cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74680-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74680-201-63400 in 1 CANISTER11/04/2024
    1NDC:74680-201-912.4 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00311/04/2024
    Labeler - Unico International Trading Corporation (805757200)
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