DR. DU-MORES VIRAL DEFENSE NANO SILVER SKIN DISINFECTANT AND 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.

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Dr. Du-More's VIRAL DEFENSE Nano Silver SKIN DISINFECTANT AND PROTECTANT

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.

FRAGRANCE-FREE

NON-ALCOHOL, WATER-BASED

ANTI-MICROBIAL PROTECTION

DOESN'T DRY OR CRACK SKIN

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

12 HOUR SKIN PROTECTION

**use as directed at www.doctordumore.com

Manufactured by:

Core Pacific, Inc.

4000 Leeland, Street

Houston TX 77023

www.corepacificinc.com

1-800-860-1637

MADE IN USA.

Packaging

IMAGEIMAGE

DR. DU-MORES VIRAL DEFENSE NANO SILVER SKIN DISINFECTANT AND PROTECTANT 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79518-088
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:79518-088-0159.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/01/2020
2NDC:79518-088-02237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/01/2020
Labeler - Core Pacific, Inc. (022106593)
Establishment
NameAddressID/FEIBusiness Operations
Core Pacific, Inc.022106593manufacture(79518-088)

Revised: 11/2020
Document Id: 4f9ddfb9-60b1-4cb6-8d97-0c36fecc73bb
Set id: 1d8a4849-1af9-49b5-a711-4d8d7038ed09
Version: 1
Effective Time: 20201107
 
Core Pacific, Inc.