Label: TOUGH GUY 821 ANTIMICROBIAL LIQUID LTION SO AP- chloroxylenol liquid

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

Drug Label Information

Updated December 18, 2024

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  • Active ingredient

    Chloroxylenol 0.3%

  • Purpose

    Antimicrobial

  • Use

    • Handwash to help decrease bacteria on the skin

    • Recommended for repeated use

  • Warnings

    For external use only

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor ifirritation or rash appears and lasts

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

  • Directions

    • Wet hands

    • Apply a small amount of product and work into a lather

    • Rinse well and dry hands completely

  • Inactive ingredients

    Water (Aqua), Coconut Acid, Oleic Acid, Sodium Sulfate, Ethanolamine, Cocamide MEA, Coco-Betaine, Propylene Glycol, Retinyl Palmitate, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Hydroxypropyl Methylcellulose, Fragrance (Parfum)

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    TOUGH GUY 821 ANTIMICROBIAL LIQUID LTION SO AP 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:40096-0051
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.003 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCONUT ACID (UNII: 40U37V505D)  
    OLEIC ACID (UNII: 2UMI9U37CP)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    MONOETHANOLAMINE (UNII: 5KV86114PT)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CORN OIL (UNII: 8470G57WFM)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:40096-0051-13780 mL in 1 PACKAGE; Type 0: Not a Combination Product10/30/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/30/2008
    Labeler - W.W. GRAINGER, INC. (005103494)
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