Label: ZEP APPLAUD AB- chloroxylenol liquid

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

Drug Label Information

Updated October 20, 2023

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  • Active Ingredient

    Chloroxylenol 0.3%

  • Purpose

    Antiseptic

  • Uses

    Hand washing to decrease bacteria on skin.

  • Warnings

    • For external use only.
  • Do not use

    Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

  • When using this product

    • Do not swallow.
    • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.
  • Stop use ask a doctor

    Stop use ask a doctor if skin irritation or redness persists for more than 72 hours.

  • Keep out of reach of children

    Keep out of reach of children except under adult supervision.

  • Directions

    • Wet hands with water.
    • Place hands under dispenser.
    • Apply liquid soap.
    • Massage soap into hands and wrists, emphasizing back of hands, knuckles, and cuticles.
    • Rinse thoroughly.
  • Other information

    • Store at room temperature.
    • Do not freeze.
    • Dispose in accordance with all applicable federal, state and local regulations.
  • Inactive ingredients

    Water, Potassium Oleate , Cocamide DIPA, Lauric Acid, Sodium Chloride, Tetrasodium EDTA, Acrylates/PEG-10 maleate/Styrene Copolymer, Isopropyl Alcohol, Fragrance, BHT, Red 4, Red 33

  • Questions or comments?

    Call 1-877-BUY-ZEP (1-877-428-9937)

  • PRINCIPAL DISPLAY PANEL

    123_3385

  • INGREDIENTS AND APPEARANCE
    ZEP APPLAUD AB 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-123
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURIC ACID (UNII: 1160N9NU9U)  
    POTASSIUM OLEATE (UNII: 74WHF607EU)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-123-2415140 mL in 1 CASE; Type 0: Not a Combination Product03/10/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/10/2017
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-123)
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