Label: V3 VIRAL DEFENSE NANO SILVER SKIN PROTECTANT- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL

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 July 17, 2020

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  • DRUG FACTS

  • ACTIVE INGREDIENT

    Benzalkonium Chloride 0.1%

  • PURPOSE

    Antimicrobial

  • INDICATIONS & USAGE

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

  • WARNINGS

    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.

  • DOSAGE & ADMINISTRATION

    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.

  • INACTIVE INGREDIENT

    Other Ingredients: structured water, nano colloidal silver, organosilane, sodium sesquicarbonate, fulvic acid, magnesium

  • SPL UNCLASSIFIED SECTION

    • NON-ALCOHOL

    • GUARDS AGAINST INFECTION

    • ECO-FRIENDLY

    • DOESN'T DRY OR CRACK YOUR SKIN

    99.99% EFFECTIVE AGAINST BACTERIA, VIRUSES & MOST COMMON GERMS.

    24 HOUR SKIN PROTECTION

    POWERED BY: V3 PROPRIETARY TECHNOLOGY

    Manufactured by:

    Core Pacific, Inc for

    V3 International Inc.

    4000 Leeland St

    Houston, TX 77003

    www.v3viraldefense.com

    1-888-462-4928   

    MADE IN USA.

  • Packaging

    IMAGE1IMAGE2IMAGE3IMAGE5IMAGE4IMAGE6

  • INGREDIENTS AND APPEARANCE
    V3 VIRAL DEFENSE NANO SILVER SKIN PROTECTANT 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79518-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SILVER (UNII: 3M4G523W1G)  
    .GAMMA.-METHACRYLOXYPROPYLTRIMETHOXYSILANE (UNII: JV48X1M2EQ)  
    SODIUM SESQUICARBONATE (UNII: Y1X815621J)  
    FULVIC ACID (UNII: XII14C5FXV)  
    MAGNESIUM (UNII: I38ZP9992A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79518-100-0159.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/01/2020
    2NDC:79518-100-02250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/01/2020
    3NDC:79518-100-031000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/01/2020
    4NDC:79518-100-043785 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    5NDC:79518-100-05208198 mL in 1 DRUM; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/01/2020
    Labeler - Core Pacific, Inc. (022106593)
    Establishment
    NameAddressID/FEIBusiness Operations
    Core Pacific, Inc.022106593manufacture(79518-100)
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