Label: XHC-79- ethyl alcohol solution

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 19, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active ingredient

    Ethyl Alcohol 62.0% w/w (equivalent to 68.4% v/v)

  • Purpose

    Antiseptic handwash

  • Uses

    • for hand washing to decrease bacteria on the skin
  • Warnings

    • For external use only
    • Flammable, keep away from fire or flame, heat sparks and sources of static discharge.

    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 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 thoroughly with product and allow to dry without wiping.
    • do not use if hands are visibly dirty or greasy; wash hands with soap and water instead
  • Other Information

    • for additional information, see Safety Data Sheet (SDS)
    • EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).
  • Inactive Ingredients

    water (aqua), PEG-10 dimethicone, ethylhexylglycerin, farnesol, t-butyl alcohol, bisabolol, denatonium benzoate

  • QUESTIONS

    Questions? call 1-800-35-CLEAN (352-5326)

  • Principal display panel and representative label

    ECOLAB

    47593-656-70

    XHC-79

    Active Ingredient: Ethyl Alcohol 62.0% w/w (equivalent to 68.4% v/v)

    1200 mL

    (40.6 US FL OZ)   6000355

    Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA

    © 2024 Ecolab USA Inc. · All rights reserved

    Made in United States

    www.ecolab.com · 782976/8500/0224

    SDS-MN-914, SDS-NC-872

    representative label

  • INGREDIENTS AND APPEARANCE
    XHC-79 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-656
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol68.4 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    FARNESOL (UNII: EB41QIU6JL)  
    .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-656-701200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/19/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/19/2024
    Labeler - Ecolab Inc. (006154611)