Label: DIGISAN E- benzalkonium chloride solution

  • NDC Code(s): 47593-404-30, 47593-404-41, 47593-404-59
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 28, 2024

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  • Active ingredient

    Benzalkonium chloride, 0.1%

  • 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 sparks and sources of static discharge

    Do not use

    • In eyes

    When using this product

    • Discontinue use if irritation and redness develop

    Stop use and ask a doctor if

    • Skin 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 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 (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 USA)
  • Inactive ingredients:

    water (aqua), isopropyl alcohol, propylene glycol, FD&C red 40, F&DC blue 1

  • Questions?

    Call 1-800-35-CLEAN (352-5326)

  • Principal Display Panel/Representative Label

    ECOLAB

    6123674

    DigiSan™

    E Foam Hand Sanitizer

    750 mL (25 US FL OZ)

    Active Ingredient:

    Benzalkonium chloride 0.1%

    706304/5405/1020

    This product may be patented 

    www.ecolab.com/patents

    Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326)

    5105 Tomken Road · Mississauga ON L4W 2X5 Canada

    © 2020 Ecolab USA Inc · All rights reserved

    Made in U.S.A.

    www.ecolab.com

    Representative Label

  • INGREDIENTS AND APPEARANCE
    DIGISAN E 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-404
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 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:47593-404-30207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/200303/13/2017
    2NDC:47593-404-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2003
    3NDC:47593-404-591250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/200303/13/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/04/2003
    Labeler - Ecolab Inc. (006154611)
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