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

  • NDC Code(s): 65321-039-01, 65321-039-02, 65321-039-03
  • Packager: Rubbermaid Commercial Products LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    0.13% Benzalkonium Chloride

  • Purpose

    Antiseptic Cleaner

  • 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.
  • Directions

    Place hands under the dispenser, allow 0.4 mL of foam into hands, rub thoroughly over the surface of both hands for at least 30 seconds, and then allow hands dry

  • Inactive Ingredients

    Water (Aqua), Propylene Glycol, PEG-6 Caprylic/Capric Glycerides, Phenoxyethanol, Decylamine Oxide, Tetrasodium Glutamate Diacetate, Sodium Hydroxide, Caprylyl Glycol, Ethylhexylglycerin, Lactic Acid, Shea Butteramidopropyl Betaine, Sodium Chloride, Hexylene Glycol, Benzoic Acid, Tocopherol, 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 - 1100 mL Pouch Label

    Rubbermaid®
    Commercial Products

    Enriched Foam Alcohol-Free Hand Sanitizer
    With Shea Butter & Vitamin E

    NSF®

    Nonfood Compounds
    Program Listed E3
    NSF Registration #143589

    1100 mL (37.2 FL. OZ. U.S.)

    © 2021 | 2147031 | PRFR11080 FRONT
    PRFR11080 V-06-2021 FRONT

    PRINCIPAL DISPLAY PANEL - 1100 mL Pouch Label
  • INGREDIENTS AND APPEARANCE
    ENRICHED FOAM ALCOHOL-FREE HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65321-039
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 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)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65321-039-014 in 1 BOX06/21/2021
    11100 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:65321-039-024 in 1 BOX06/21/2021
    21300 mL in 1 POUCH; Type 0: Not a Combination Product
    3NDC:65321-039-036 in 1 BOX06/21/2021
    3800 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH DRUGM00406/21/2021
    Labeler - Rubbermaid Commercial Products LLC (049924368)
    Establishment
    NameAddressID/FEIBusiness Operations
    NWL Netherlands Services B.V.494692088ANALYSIS(65321-039) , MANUFACTURE(65321-039)
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