Label: ECOLAB- ethyl alcohol solution

  • NDC Code(s): 47593-489-26, 47593-489-31, 47593-489-33, 47593-489-49, view more
    47593-489-55
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated April 26, 2024

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

  • Active Ingredient

    Ethyl Alcohol 62% w/w

  • Purpose

    Antiseptic handwash

  • Uses

    • For handwashing to decrease bacteria on the skin
  • Warnings

    • For external use only
    • Flammable, keep away from fire or flame, heat, sparts 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 doctor if

    • Skin irritation or redness persists 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 dry
  • Other information

    • for additional information, see Material Safety Data Sheet (MSDS)
    • for emergency medical information in USA and Canada, call 1 800 328 0026
  • INACTIVE INGREDIENT

    Inactive ingredients water (aqua), glycerin, tetrahydroxyethyl ethylenediamine, ethylhexylglycerin, isopropyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, C12-C15 alkyl benzoate, panthenol, tert-butyl alcohol, tocopheryl acetate, dimethicone, aloe barbadensis leaf juice, denatonium benzoate

  • QUESTIONS

    Questions? call 1 866 781 8787

  • Representative Label and Principal Display Panel

    ECOLAB®

    NDC 47593-489-55

    Moisturizing Gel

    Hand Sanitizer

    Dye and Fragrance Free

    Active Ingredient: 62% Ethyl Alcohol

    Net Contents:         6084642

    1000 mL (33.8 fl oz)

    746338/8501/0912

    Ecolab · 370 Wabasha Street N · St Paul MN 55102-1390 USA

    © 2018 Ecolab USA Inc · All rights reserved

    Made in United States

    746340/8502/1218

    Representative Label

  • INGREDIENTS AND APPEARANCE
    ECOLAB 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-489
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ETHYLENEDIAMINE TETRAETHANOL (UNII: K5APE098ZI)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-489-261000 mL in 1 POUCH; Type 0: Not a Combination Product12/07/201301/05/2023
    2NDC:47593-489-33118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/07/2013
    3NDC:47593-489-4937 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/07/2013
    4NDC:47593-489-31540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/07/201301/05/2023
    5NDC:47593-489-551000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/07/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/07/2013
    Labeler - Ecolab Inc. (006154611)