V3 VIRAL DEFENSE NANO SILVER SKIN PROTECTANT- benzalkonium chloride liquid

V3 Viral Defense Nano Silver Skin Protectant by

Drug Labeling and Warnings

V3 Viral Defense Nano Silver Skin Protectant by is a Otc medication manufactured, distributed, or labeled by Core Pacific, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SILVER (UNII: 3M4G523W1G)
.GAMMA.-METHACRYLOXYPROPYLTRIMETHOXYSILANE (UNII: JV48X1M2EQ)
SODIUM SESQUICARBONATE (UNII: Y1X815621J)
FULVIC ACID (UNII: XII14C5FXV)
MAGNESIUM (UNII: I38ZP9992A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79518-100-01	59.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2020
2	NDC: 79518-100-02	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2020
3	NDC: 79518-100-03	1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2020
4	NDC: 79518-100-04	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020
5	NDC: 79518-100-05	208198 mL in 1 DRUM; Type 0: Not a Combination Product	08/01/2020

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	Business Operations
Core Pacific, Inc.		022106593	manufacture(79518-100)