Label: DIGICLEAN E- chloroxylenol solution

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

Drug Label Information

Updated March 15, 2024

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  • Active Ingredient

    Chloroxylenol, 1.0%

  • 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

    • 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 apply foam
    • Scrub hands and forearms
    • Rinse thoroughly and dry
  • Other information

    • For additional information see Safety Data Sheet (SDS)
    • For emergency medical information in USA and Canada, call 1-800-328-0026
    • For emergency medical information worldwide, call 1-651-222-5352 (in the USA)
  • Inactive ingredients

    Inactive ingredients water (aqua), propylene glycol, urea, sorbitol, potassium cocoate, tetrasodium EDTA, SD alcohol 3-C, glycerin, sodium xylenesulfonate, citric acid, fragrance, lauramine oxide, FD&C yellow 5, FD&C blue 1

  • Questions?

    Call 1.800.35.CLEAN (352.5326)

  • Principal Display Panel

    DIN 02242847

    ECOLAB

    23673

    6123673

    DigiClean™

    E Foam Hand Soap

    750 mL (25 US FL OZ)

    Active Ingredient: Chloroxylenol, 1.0%

    705708/5405/0117

    This product may be patented

    patentado: www.ecolab.com/patents

    Ecolab · 1 Ecolab Place · St. Paul MN 55102 U.S.A.

    5105 Tomken Road · Mississauga ON L4W 2X5 Canada

    © 2017 Ecolab Inc. · All Rights Reserved

    Made in United States

    705708/5405/0117

    Representative label

  • INGREDIENTS AND APPEARANCE
    DIGICLEAN E 
    chloroxylenol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-308
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL1.0 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    UREA (UNII: 8W8T17847W)  
    SORBITOL (UNII: 506T60A25R)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-308-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/1999
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/26/1999
    Labeler - Ecolab Inc. (006154611)
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