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

Dr. Du-Mores Viral Terminator Nano Silver Skin Disinfectant Hand Sanitizing by

Drug Labeling and Warnings

Dr. Du-Mores Viral Terminator Nano Silver Skin Disinfectant Hand Sanitizing 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 0.13%

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

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79518-888
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SILVER (UNII: 3M4G523W1G)
SODIUM SESQUICARBONATE (UNII: Y1X815621J)
MAGNESIUM (UNII: I38ZP9992A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79518-888-01	59.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/16/2020
2	NDC: 79518-888-02	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/16/2020

Labeler - Core Pacific, Inc. (022106593)

Establishment
Name	Address	ID/FEI	Business Operations
Core Pacific, Inc.		022106593	manufacture(79518-888)