Label: NINJA GOLDFISH SANITIZING BODY- benzalkonium chloride spray

  • NDC Code(s): 71884-102-01, 71884-102-02, 71884-102-03, 71884-102-04, view more
    71884-102-05
  • 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 October 6, 2022

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  • DRUG FACTS

  • Active Ingredient:

    Benzalkonium Chloride 0.10%

  • Purpose:

    First aid antiseptic

  • Uses:

    First aid anti-microbial - Topical body sanitizer - Preventive antiseptic

  • Directions:

    spray liberally over the entire body and personal clothing, recommended for repeat application regularly, product safe on all surfaces & fabric's.

  • Warnings:

    Do not freeze. For external use only.

    Do not use in ears, eyes or mouth.

    • 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 irritation develop and persist for more than 72 hours.

    • Keep out of reach of children.

  • Inactive Ingredients:

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

  • Questions?

    +1(888) 331-8332, M-F, 9AM-5PM (EST)

  • SPL UNCLASSIFIED SECTION

    Alcohol-Free

    Long lasting, sanitizing protection from germs for the entire body 

    KILLS 99.9% OF GERMS

    WITH SOOTHING ALOE VERA

    Formulated and enhanced with
    Zetrisil®

    FAST ACTING 15-SECOND FORMULA

    Distributed by: Ninja Goldfish
    1007 Industrial Park
    Albion, Michigan 49224
    Ph: 855-ninjafish | www.ninjagf.com

  • Packaging

    ESC-102

  • INGREDIENTS AND APPEARANCE
    NINJA GOLDFISH SANITIZING BODY 
    benzalkonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71884-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    LAURETH-4 (UNII: 6HQ855798J)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71884-102-0110 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2022
    2NDC:71884-102-0250 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2022
    3NDC:71884-102-0358 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2022
    4NDC:71884-102-04473 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2022
    5NDC:71884-102-053785 mL in 1 JUG; Type 0: Not a Combination Product09/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/01/2022
    Labeler - Enviro Specialty Chemicals Inc (202621850)
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