Label: DR. DU-MORES VIRAL TERMINATOR NANO SILVER SKIN DISINFECTANT HAND SANITIZING- benzalkonium chloride liquid

  • 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 19, 2020

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  • DRUG FACTS

  • ACTIVE INGREDIENT

    Benzalkonium Chloride 0.13%

  • PURPOSE

    Antimicrobial

  • Uses:

    Sanitizes and protects skin and surfaces to help reduce viruses and bacteria that cause disease.

  • WARNINGS:

    For external use only.

    Do not use in eyes. If contact occurs, flush thoroughly with water.

    Stop use and ask a doctor: If irritation or redness develops, or if condition persist for more than 72 hours.

    Keep out of reach of children: If swallowed, get medical help or contact a Poison Control Center.

  • DIRECTIONS:

    On dry skin, apply enough product to thoroughly cover the areas to be protected and allow to dry. If abrasively washed reapply as needed.

  • Other Ingredients:

    structured water, nano colloidal silver, sodium sesquicarbonate, magnesium

  • SPL UNCLASSIFIED SECTION

    • WATER-BASED, NON-ALCOHOL

    • GUARDS AGAINST INFECTION

    • DOESN'T DRY OR CRACK SKIN

    EFFECTIVELY REDUCE 99.9% COMMON BACTERIA, GERMS & VIRUSES INCLUDING CORONAVIRUS**

    12 HOUR SKIN PROTECTION

    **use as directed www.doctordumore.com

    Manufactured by:

    Core Pacific, Inc.

    4000 Leeland St

    Houston, TX 77023

    www.corepacificinc.com

    1-800-860-1637

    MADE IN USA.

  • Packaging

    IMAGEIMAGE

  • INGREDIENTS AND APPEARANCE
    DR. DU-MORES VIRAL TERMINATOR NANO SILVER SKIN DISINFECTANT HAND SANITIZING 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79518-888
    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
    WATER (UNII: 059QF0KO0R)  
    SILVER (UNII: 3M4G523W1G)  
    SODIUM SESQUICARBONATE (UNII: Y1X815621J)  
    MAGNESIUM (UNII: I38ZP9992A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79518-888-0159.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/16/2020
    2NDC:79518-888-02237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/16/2020
    Labeler - Core Pacific, Inc. (022106593)
    Establishment
    NameAddressID/FEIBusiness Operations
    Core Pacific, Inc.022106593manufacture(79518-888)
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