OTC Medication Information: V3 Viral Defense Nano Silver Skin Protectant

V3 VIRAL DEFENSE NANO SILVER SKIN PROTECTANT- benzalkonium chloride liquid
Core Pacific, Inc.

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 FACTS

ACTIVE INGREDIENT

Benzalkonium Chloride 0.1%

PURPOSE

Antimicrobial

Uses: Sanitizes and protects skin 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, organosilane, sodium sesquicarbonate, fulvic acid, magnesium

• 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

V3 VIRAL DEFENSE NANO SILVER SKIN PROTECTANT benzalkonium chloride liquid

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79518-100 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.1 g in 100 mL

Inactive Ingredients Ingredient Name Strength WATER SILVER .GAMMA.-METHACRYLOXYPROPYLTRIMETHOXYSILANE SODIUM SESQUICARBONATE FULVIC ACID MAGNESIUM

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:79518-100-01 59.14 mL in 1 BOTTLE, SPRAY None 2 NDC:79518-100-02 250 mL in 1 BOTTLE, SPRAY None 3 NDC:79518-100-03 1000 mL in 1 BOTTLE, SPRAY None 4 NDC:79518-100-04 3785 mL in 1 BOTTLE None 5 NDC:79518-100-05 208198 mL in 1 DRUM None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/01/2020

Labeler — Core Pacific, Inc. (022106593)

Establishment
Name	Address	ID/FEI	Operations
Core Pacific, Inc.		022106593	manufacture (79518-100)

Revised: 07/2020 Core Pacific, Inc.