Label: QUIK-CARE- ethyl alcohol solution

  • NDC Code(s): 47593-491-38, 47593-491-41, 47593-491-55, 47593-491-56, view more
    47593-491-57, 47593-491-85
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated April 26, 2024

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  • Active ingredient

    Ethyl alcohol, 62% w/w

  • 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

    • Apply product onto hands, spread thoroughly and rub until dry
  • Other Information

    • for additional information, see Safety Data Sheet (SDS)
    • for emergency medical information in USA and Canada, call 1.800.328.0026
  • Inactive Ingredients

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

  • QUESTIONS

    Questions? call 1.866.781.8787 24 hours a day, 7 days a week

  • Principal display panel and representative label

    NDC 47593-491-41

    ECOLAB®

    QUIK-CARE™

    Foam Hand Sanitizer

    Dye and Fragrance Free

    CHG Compatible

    Active Ingredient: 62% Ethyl Alcohol

    Net Contents: 750mL (25 fl oz)

    6000073

    This product may be patented: www.ecolab.com/patents

    Ecolab · 1 Ecolab Place · St Paul MN 55102 USA

    © 2020 Ecolab USA Inc · All rights reserved

    Made in United States

    www.ecolab.com - 755128/8504/1220

    SDS-WI-15014, SDS-NJ-20007, SDA-MA-1396, SDS-NC-872

    representative label

  • INGREDIENTS AND APPEARANCE
    QUIK-CARE 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-491
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol539.71 mg  in 1 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:47593-491-551000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/19/2013
    2NDC:47593-491-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/19/2013
    3NDC:47593-491-38500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/19/201312/20/2023
    4NDC:47593-491-8545 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/29/2014
    5NDC:47593-491-561200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/19/2013
    6NDC:47593-491-57535 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/09/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/19/2013
    Labeler - Ecolab Inc. (006154611)
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