Label: TORK HAND SANITIZER ALCOHOL FREE FOAM- benzalkonium chloride liquid

  • NDC Code(s): 49351-103-01
  • Packager: Essity Professional Hygiene North America LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 2, 2024

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium chloride, 0.13%

  • Purpose

    Antiseptic

  • Uses

    Handwash to help reduce bacteria on the skin.

  • Warnings

    • For external use only
    • Do not ingest
    • Avoid contact with the eyes

    Ask a doctor before use if you have:

    Deep wounds, animal bites or serious burns

    Stop use and ask a doctor:

    If irritation and redness develop.

    Keep out of reach of children:

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    Dispense enough to spread on both hands to wrists, then rub into the skin for at least 30 seconds.  Allow to dry.

  • Inactive ingredients

    Water/Eau/Aqua, Lactic acid, Triethanolamine, Cocoamidopropyl betaine, 2-Phenoxyethanol, Propano-1,2-diol, Sodium cocoamphoacetate.

  • Questions or Comments?

    1-866-722-8675

  • PRINCIPAL DISPLAY PANEL

    TORK®

    Hand Sanitizer

    Alcohol Free Foam

    Benzalkonium Chloride, 0.13%

    NDC 49351-103-01

    Manufactured for Essity Professional Hygiene North America, LLC

    2929 Arch Street

    Philadelphia, PA 19104

    www essity.com, www.torkusa.com

    For Commercial use

    Made in Mexico

    Premium

    1 L

    (33.8 US fl. oz.)

    (35.2 oz. liq.)

    Tork BZK sanitizer foam Label.jpg

  • INGREDIENTS AND APPEARANCE
    TORK HAND SANITIZER ALCOHOL FREE FOAM 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49351-103
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49351-103-016 in 1 BOX10/15/2018
    11000 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/12/2014
    Labeler - Essity Professional Hygiene North America LLC (005694349)