Label: KAY MCD- chloroxylenol solution

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

Drug Label Information

Updated August 12, 2024

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  • Active ingredient

    Chloroxylenol 0.5%

  • Purpose

    Antiseptic handwash

  • Uses

    • For handwashing to decrease bacteria on the skin.
  • Warnings

    • For external use only

    Do not use

    • In eyes.

    When using this product

    • If in eyes, rinse promptly and thoroughly with water.
    • Discontinue use if irritation and redness develop.

    Stop use and ask a doctor if

    • Skin irritation and redness occurs for more than 72 hours.

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

  • Directions

    • Wet hands and forearms.
    • Apply 5 ml (teaspoonful) or palmful to hands and forearms.
    • Scrub thoroughly for 20 seconds.
    • Rinse and repeat.
  • Other information

    • For additional information, see Material Safety Data Sheet (MSDS)
    • For emergency medical information in USA call (877) 231-2615 or call collect 0 (952)853-1713.
  • Inactive ingredients

    water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, hydroxyethylcellulose, glycerine, coco glucoside, glyceryl oleate, citric acid, fragrance, methylchloroisothiazolinone, methylisothiazolinone, FD&C Red 40, FD&C Yellow 5, D&C Red 33.

  • Questions?

    Call 1-800-529-5458

  • Principal Display Panel - Representative Label

    NDC No.: 63146-102-01

    McD

    Anti-Microbial

    Handwash (AMH)

    FOR INSTITUTIONAL USE ONLY

    (Chloroxylenol 0.5%)

    1 US gal (3.8L)

    ECOLAB

    KAY CHEMICAL COMPANY - 8300 Capital Drive - Greensboro, NC 27409-9790 USA

    Customer Service: (800) 529-5458

    Made in USA

    Representative label

  • INGREDIENTS AND APPEARANCE
    KAY MCD 
    chloroxylenol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.5 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    HYDROXYETHYL CELLULOSE (3000 MPA.S AT 1%) (UNII: 7Q6P4JN1QT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63146-102-013800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/13/2005
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/13/2005
    Labeler - Kay Chemical Company (003237021)
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