Label: ELIMISHIELD HUNT CORE BODY FOAM FOR HUNTERS- benzalkonium chloride aerosol, foam

  • NDC Code(s): 71853-010-00
  • Packager: Bryson Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2023

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  • Drug Facts

  • Active Ingredient

    Benzalkonium chloride 0.13%

    Purpose

    Antiseptic Skin Sanitizer

  • Uses

    • Sanitizer to help decrease bacteria on the skin.
    • Recommended for repeated use.
  • Warnings

     For external use only.

    • Do not use in ears or mouth and avoid mucus membranes.

    When using this product

    • Avoid contact with the eyes.
    • In case of contact flush eyes with water.

    Stop use and ask a doctor if

    redness or iirtation develops and persist for more than 72 hours.

    Keep out of reach of children.

    Children should be supervised when using this product.

  • Directions

    • Apply a small amount into palms of hands and spread throughout body.
    • Rub into skin until dry.
  • Inactive Ingredients

    Aloe Barbadensis Leaf Juice extract.Caprylyl Glucoside, Citric Acid, Glycerin, Laureth-4, 1-Octadecanaminium NN Dimethyl (3-Trimethoxysilyl) Propyl Chloride, Phenoxyethanol, Polyaminopropyl biguanide, Water.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    ELIMISHIELD HUNT CORE BODY FOAM FOR HUNTERS 
    benzalkonium chloride aerosol, foam
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71853-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURETH-4 (UNII: 6HQ855798J)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71853-010-00200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/01/2020
    Labeler - Bryson Industries, Inc. (040363256)
    Establishment
    NameAddressID/FEIBusiness Operations
    Filltech USA, LLC926433855manufacture(71853-010)
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