Label: KAY RTU FOAMING AB HANDSOAP- chloroxylenol solution

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

Drug Label Information

Updated March 4, 2025

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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 to remove soil
    • Dispense palmful
    • spread to cover hands, rub in well
    • air dry, do not rinse or towel dry
  • Other Information

    • for additional information, see Safety Data Sheet (SDS)
    • EMERGENCY HEALTH INFORMATION: 1 877 231 2615. If located outside the United States and Canada, call collect 952 853 1713 (number is in the US).
  • INACTIVE INGREDIENT

    Inactive ingredients water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, caprylyl/capryl glucoside, fragrance, lauryl glucoside, red 40, methylchloroisothiazolinone, yellow 5, methylisothiazolinone

  • QUESTIONS

    Questions?  Call 1-800-529-5458

  • Principal display panel and representative label

    ECOLAB

    Kay RTU Foaming AB Hand Soap

    Active Ingredient: Chloroxylenol 0.5%

    1200 mL

    (40.6 US FL OZ)

    1112847

    Kay Chemical Company · 8300 Capital Drive

    Greensboro, NC 27409-9790 USA

    Customer Service: (800) 529-5458

    ©2025 Kay Chemical Company

    All rights reserved

    KUSA · 783800/8000/0225

    representative label

  • INGREDIENTS AND APPEARANCE
    KAY RTU FOAMING AB HANDSOAP 
    chloroxylenol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-321
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLYL/CAPRYL GLUCOSIDE (UNII: E00JL9G9K0)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63146-321-161200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/04/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/04/2025
    Labeler - Kay Chemical Co. (003237021)
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