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Knuckle Under Medicated (Betco Corporation, Ltd.)

Available Formats

Dosage Form Package Information Links
SOAP 1100 mL in 1 BAG (65601-765-10) Label Information
SOAP 3780 mL in 1 BOTTLE, PLASTIC (65601-765-04) Label Information
SOAP 900 mL in 1 BAG (65601-765-19) Label Information

Complete Knuckle Under Medicated Information

  • Knuckle Under Medicated

    ​Active Ingredient

    ​ ​Chloroxylenol 0.5%


  • Knuckle Under Medicated

    Uses

    • ​​For use in a variety of industrial setting including manufacturing, machine shops, maintenance areas and automotive shops.

  • Knuckle Under Medicated

    Warnings

    • For external use only.
    • Avoid contact with eyes.
    • If contact occurs, rinse thoroughly with water.
    • Discontinue use is irritation or redness develops.
    • If irritation persists for more than 72 hours, consult a physician.
    • KEEP OUT OF REACH OF CHILDREN.
    • If swallowed, get medical help or contact a poison control center right away.

  • Knuckle Under Medicated

    Directions

    • ​Read the entire label before using this product.
    • ​Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands..
    • Rinse with clean water.

  • Knuckle Under Medicated

    Inactive Ingredients

    ​Water, sodium tallate, Sodium Laureth Sulfate, Triisopropanolamine, Alcohol, Tetrasodium EDTA, Sodium Chloride, Coco MIPA, Fragrance,  Cocamidopropropyl Betaine, Glycerin, Methyl Chlorosiothiazolinone, D&C Green #5, FD&C Yellow #5.


  • Knuckle Under Medicated

    Purpose

    Antibacterial


  • Knuckle Under Medicated

    KEEP OUT OF REACH OF CHILDREN


  • Knuckle Under Medicated

    765.jpg


  • INGREDIENTS AND APPEARANCE
    KNUCKLE UNDER MEDICATED 
    chloroxylenol soap
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:65601-765
    Route of Administration Topical
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 5.0 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    TALL OIL ACID (UNII: H9HR63474M)  
    TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)  
    ALCOHOL (UNII: 3K9958V90M)  
    TRIMETHYLENEDIAMINETETRAACETIC ACID (UNII: 3F6OA94EER)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65601-765-19 900 mL in 1 BAG; Type 0: Not a Combination Product 11/12/2012 01/01/2016
    2 NDC:65601-765-10 1100 mL in 1 BAG; Type 0: Not a Combination Product 11/12/2012 01/01/2016
    3 NDC:65601-765-04 3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2016
    4 NDC:65601-765-06 3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/12/2012
    5 NDC:65601-765-55 208000 mL in 1 DRUM; Type 0: Not a Combination Product 11/12/2012
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 11/12/2012
    Labeler - Betco Corporation, Ltd. (070307547)
    Registrant - Betco corporation, Ltd. (070307547)
    Establishment
    Name Address ID/FEI Business Operations
    Betco Corporation, Ltd. 070307547 manufacture(65601-765) , label(65601-765) , pack(65601-765)