Label: MCD- chloroxylenol solution

  • NDC Code(s): 63146-108-03, 63146-108-10
  • Packager: Kay Chemical Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 16, 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 or 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 palmful of to hands and forearms
    • Scrub thoroughly • Rinse and dry
  • Other Information

    • for additional information, see Safety Data Sheet (SDS)
    • Medical Emergency: (877) 231-2615 or call collect 0 (952) 853-1713
  • INACTIVE INGREDIENT

    Inactive ingredients:  water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, citric acid, coco-glucoside, glyceryl oleate, fragrance, methylchloroisothiazolinone, CI 19140 (FDC Yellow No. 5), methylisothiazolinone, CI 14700 (FDC Red No. 4)

  • QUESTIONS

    Questions?  Call 1-800-529-5458

  • Principal display panel and representative label

    NDC 63146-108-10

    Kay®

    Peel Here For Drug Facts

    McD® Foaming

    Antibacterial Hand Soap

    Instant foam lathers fast •Mild, pH-balanced formula •Fresh, clean fragrance

    McD® Foaming Antibacterial Hand Soap is a rich lather hand soap with a balanced blend of cleaning agents and skin protecting moisturizers.

    KEEP OUT OF REACH OF CHILDREN • FOR INSTITUTIONAL USE ONLY

    Chloroxylenol 0.5%

    To obtain Spanish Instructions, see outer carton.

    Net contents: 42 US fl oz (1250 mL)

    Distributed by:

    KAY CHEMICAL COMPANY•8300 Capital Drive

    Greensboro, NC 27409-9790, USA

    Customer Service:  (800) 529-5458

    ®2015 Kay Chemical Company

    All rights reserved

    763982-00•McDUSA 763982/8000/1115

    representative label

  • INGREDIENTS AND APPEARANCE
    MCD 
    chloroxylenol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-108
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    COCO-GLUCOSIDE (UNII: ICS790225B)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63146-108-03750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/17/200709/18/2019
    2NDC:63146-108-101250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/17/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/17/2007
    Labeler - Kay Chemical Company (003237021)
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