Label: DOCTOR INKS HAND SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 71884-201-01, 71884-201-02, 71884-201-03, 71884-201-04, view more
    71884-201-05, 71884-201-06
  • 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 February 14, 2023

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  • Drug Facts

  • Active Ingredient:

    Benzalkonium Chloride 0.13%

  • Purpose:

    Antiseptic, Hand & Skin Sanitizer

  • Uses:

    Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use.

  • 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.
    • Children should be supervised when using this product.
  • Directions:

    Apply liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat use.

  • 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

    Long-lasting, alcohol-free protection from germs

    Formulated and enhanced with Zetrisil®

    Kills 99.9% of Germs

    Alcohol Free

    Contains Soothing Aloe Vera

    Fast-acting
    15-Second Formula

    Foaming Pump Top

    Distributed by:
    ESC Brands, LLC.
    1060 Blue Prince Road
    Bluefield, WV 24701
    www.doctor-ink.com

    FORMULATED IN THE USA

    MADE IN CHINA

  • Packaging

    sanitizerfoam

  • INGREDIENTS AND APPEARANCE
    DOCTOR INKS HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71884-201
    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)  
    WATER (UNII: 059QF0KO0R)  
    LAURETH-4 (UNII: 6HQ855798J)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71884-201-0158 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
    2NDC:71884-201-02118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
    3NDC:71884-201-03244 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
    4NDC:71884-201-04473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
    5NDC:71884-201-051182 mL in 1 BAG; Type 0: Not a Combination Product09/01/2022
    6NDC:71884-201-063785 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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