Label: KEYSTONE- benzalkonium chloride solution

  • NDC Code(s): 47593-359-41, 47593-359-56
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 19, 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

    Do not use

    • in eyes

    When using this product

    • discontinue use if irritation and redness develop

    Stop use and ask a doctor if

    irritation and redness develop

  • KEEP OUT OF REACH OF CHILDREN

    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 20 mL into hand (palmful)
    • spread to cover hands, rub in well for at least 30 seconds
    • 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 the USA)
  • INACTIVE INGREDIENT

    Inactive ingredients  water (aqua), isopropyl alcohol, propylene glycol, red 40, blue 1

  • Questions?

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

  • Primary Display Panel / Representative label

    KEYSTONE   SYSCO

    FOAM HAND SANITIZER

    Active Ingredient: Benzalkonium chloride 0.1%

    Sysco 7715473 6100098 ECOLAB

    750 ML (25 US FL OZ)

    Distributed by

    Sysco Corporation

    Manufactured by:

    Ecolab - 1 Ecolab Place - St. Paul MN 55102

    tel: 1 800 35 CLEAN (352 5326)

    (c) 2021 Ecolab USA Inc - All rights reserved

    Made in U.S.A.

    representative label

  • INGREDIENTS AND APPEARANCE
    KEYSTONE  
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-359
    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:47593-359-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/26/2002
    2NDC:47593-359-561200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/26/2002
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/26/2002
    Labeler - Ecolab Inc. (006154611)
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