Label: TC ALCOHOL-FREE HAND SANITIZER- benzethonium chloride liquid

  • NDC Code(s): 65321-034-01, 65321-034-02
  • Packager: Rubbermaid Commercial Products LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 29, 2019

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    0.1% Benzethonium Chloride

  • Purpose

    Antiseptic

  • Use

    To decrease potentially harmful germs on skin.

  • Warnings

    • For external use only.

    • When using this product avoid contact with eyes. In case of eye contact, flush with water.

    • Stop use and ask a doctor, if irritation or redness persist.

    • Do not ingest.

    • Keep out of reach of children, if swallowed, get medical help or contact a Poison Control Center right away.

    • READ MATERIAL SAFETY DATA SHEET BEFORE USING PRODUCT.
  • Directions

    Apply generously to hands. Rub hands together. Allow hands to dry. Repeat daily as necessary.

  • Inactive Ingredients

    Water (Aqua), Propylene Glycol, PEG-6 Caprylic/Capric Glycerides, Phenoxyethanol, Decylamine Oxide, Tetrasodium Glutamate Diacetate, Sodium Hydroxide, Caprylyl Glycol, Ethylhexylglycerin, Lactic Acid, Disodium Lauriminodipropionate Tocopheryl Phosphates, Benzoic Acid, Dehydroacetic Acid, Shea Butteramidopropyl Betaine, Hexylene Glycol, Sodium Citrate.

  • Questions?

    1-800-347-9800 Mon–Fri, 8 AM–5 PM EST

  • SPL UNCLASSIFIED SECTION

    Distributed by
    Rubbermaid Commercial Products LLC
    3124 Valley Avenue
    Winchester, VA U.S.A. 22601-2694

  • PRINCIPAL DISPLAY PANEL - 800 mL Pouch Box

    Rubbermaid®
    Commercial Products
    TECHNICAL CONCEPTS

    Alcohol-Free Hand Sanitizer

    800 mL (27 FL. OZ. U.S.)

    PRINCIPAL DISPLAY PANEL - 800 mL Pouch Box
  • INGREDIENTS AND APPEARANCE
    TC ALCOHOL-FREE HAND SANITIZER 
    benzethonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65321-034
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.1 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DECYLAMINE OXIDE (UNII: G387VUT5EZ)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATES (UNII: 0K5Y9U1P6M)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65321-034-014 in 1 BOX10/28/201910/12/2023
    1800 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:65321-034-024 in 1 BOX10/28/201910/12/2023
    21100 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00410/28/2019
    Labeler - Rubbermaid Commercial Products LLC (049924368)
    Establishment
    NameAddressID/FEIBusiness Operations
    NWL Netherlands Production BV489421698ANALYSIS(65321-034) , MANUFACTURE(65321-034)