Label: WIPEX- antibacterial wipe cloth

  • NDC Code(s): 74680-201-86, 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

  • Keep our of the reach of children

    Keep out of the reach of children, except with adult supervision.

  • Warnings

    For external use only. Do not use in the eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult a doctor if irritation continues for more than 72 hours. If swallowed seek medical attention or call a poison control center.

  • Inactive ingredients

    Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Charmomilla Recutita (Matricaria),Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate

  • Purpose

    Antibacterial

  • To dispense

    Locate tear-notch on top of refill pouch. Tear straight across to open. Pull first wipe from center of roll through the pouch center opening. Thread wipe through dispenser nozzle. Use only upward pull dispensers.

  • To use

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

  • PRINCIPAL DISPLAY PANEL

    Wipex 800 refill

  • 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
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74680-201-86800 in 1 CANISTER03/22/2024
    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 DrugM00303/22/2024
    Labeler - Unico International Trading Corporation (805757200)
    Registrant - Dan Mor (514523067)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dan Mor514523067manufacture(74680-201)
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