Label: FOODSERVICE FOAM HAND SANITIZER- benzalkonium chloride solution

  • NDC Code(s): 47593-470-41, 47593-470-56, 47593-470-59
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 17, 2024

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  • Active ingredient

    Benzalkonium chloride 0.1%

  • Purpose

    Antiseptic handwash

  • INDICATIONS & USAGE

    • 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 throughly 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

    • wash 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 (MSDS)
    • 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 INGREDIENT

    Inactive ingredients water, propylene glycol, isopropyl alcohol, FD&C red 40, FD&C blue1

  • QUESTIONS

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

  • Principal display panel and representative container

    Ecolab

    6100730

    Foodservice Foam Hand Santiizer

    1250 mL (42.3 US FL OZ)

    Active ingredient: 

    Benzalkonium chloride 0.1%

    755555/5402/0920

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

    tel: 1 800 35 CLEAN (352 5326)

    (c) 2020 Ecolab USA Inc - All rights reserved

    Made in U.S.A.

    www.ecolab.com

    representative label

  • INGREDIENTS AND APPEARANCE
    FOODSERVICE FOAM HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-470
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-470-561200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/08/2010
    2NDC:47593-470-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2016
    3NDC:47593-470-591250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/08/2010
    Labeler - Ecolab Inc. (006154611)
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