FDA.reportPublic FDA data

Dr. Du-Mores Viral Defense Nano Silver Skin Disinfectant and Protectant

Manufacturer
Core Pacific, Inc.
Effective date
2020-11-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:23

Label at a glance#

ProductDr. Du-Mores Viral Defense Nano Silver Skin Disinfectant and Protectant
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

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

Dosage and administration

On dry skin, apply enough product to thoroughly cover the areas to be protected and allow to dry. If abrasively washed reapply as needed.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

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

WARNINGS:

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: If swallowed, get medical help or contact a Poison Control Center.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INACTIVE INGREDIENT SECTION

Structured water, nano colloidal silver, sodium sesquicarbonate, magnesium.

SPL UNCLASSIFIED SECTION

• 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD1
1049254benzalkonium chloride 0.13 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79518-088-012022-01-28C16284748780-1d6a99b39-6561-a426-e053-dadaa90af4c2Dr. Du-More's VIRAL DEFENSE Nano Silver SKIN DISINFECTANT AND PROTECTANT
79518-088-022022-01-28C16284748780-1d6a99b39-6561-a426-e053-dadaa90af4c2Dr. Du-More's VIRAL DEFENSE Nano Silver SKIN DISINFECTANT AND PROTECTANT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79518-088-01Dr. Du-Mores Viral Defense Nano Silver Skin Disinfectant and Protectant59.14 mL in 1 BOTTLE, SPRAYLIQUID59.141
79518-088-02Dr. Du-Mores Viral Defense Nano Silver Skin Disinfectant and Protectant237 mL in 1 BOTTLE, SPRAYLIQUID2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79518-088DR. DU-MORES VIRAL DEFENSE NANO SILVER SKIN DISINFECTANT AND PROTECTANT (BENZALKONIUM CHLORIDE) LIQUID [CORE PACIFIC, INC.]1Legacy NDC, 2 package rows20201112_1d8a4849-1af9-49b5-a711-4d8d7038ed09.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79518-08879518-088-01, 79518-088-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
SILVER3M4G523W1GIACT
SODIUM SESQUICARBONATEY1X815621JIACT
MAGNESIUMI38ZP9992AIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4f9ddfb9-60b1-4cb6-8d97-0c36fecc73bb1d8a4849-1af9-49b5-a711-4d8d7038ed092020-11-07WarningsExact identifier
spl id: 4f9ddfb9-60b1-4cb6-8d97-0c36fecc73bb
spl set id: 1d8a4849-1af9-49b5-a711-4d8d7038ed09

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.