Label: GERMFREE24 HAND SANITIZER- benzalkonium chloride spray

  • NDC Code(s): 71884-016-01, 71884-016-02, 71884-016-03, 71884-016-04, view more
    71884-016-05, 71884-016-06
  • Packager: Enviro Specialty Chemicals Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 17, 2020

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  • DRUG FACTS

  • Active Ingredient:

    Benzalkonium Chloride 0.13%

  • Purpose:

    Antiseptic/Hand & Skin Sanitizer

  • Directions:

    Spray liberally on the palms of the hands. Rub into the skin until dry. Recommended for repeat use.

  • Uses:

    Hand Sanitizer to help decrease bacteria on the skin.

  • Warnings:

    Do not freeze. For external use only.

    Do not use in ears, eyes or mouth.

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

    • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

    • Keep out of reach of children.

    • Children should be supervised when using this product.

  • Inactive Ingredients:

    Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

  • Questions?

    +1(888) 331-8332, Mon-Fri 9:00AM-5:00PM (EST)

  • SPL UNCLASSIFIED SECTION

    Long-lasting, alcohol-free protection from germs

    KILLS 99.99% OF GERMS

    FAST ACTING 15 SEC FORMULA

    Formulated and enhanced with Zetrisil®

    WITH SOOTHING ALOE VERA

    Distributed by: ESC Brands, LLC.

    664 Old Hargrave Road - Suite B

    Lexington, NC 27295

    ESC BRANDS

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    GERMFREE24 HAND SANITIZER 
    benzalkonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71884-016
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
    LAURETH-4 (UNII: 6HQ855798J)  
    POLIHEXANIDE (UNII: 322U039GMF)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71884-016-0110 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    2NDC:71884-016-0257 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    3NDC:71884-016-03200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    4NDC:71884-016-04250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    5NDC:71884-016-05473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    6NDC:71884-016-063785 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/17/2020
    Labeler - Enviro Specialty Chemicals Inc (202621850)
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