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

Manufacturer: Core Pacific, Inc.
Effective date: 2020-10-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:32:36

Label at a glance#

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

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.

Contacts and useful links#

PhoneLabel contact1-800-860-1637

Websitewww.doctordumore.com

www.doctordumore.com

Websitewww.corepacificinc.com

www.corepacificinc.com

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

• 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1049254	benzalkonium chloride 0.13 % Topical Solution	PSN	1
1049254	benzalkonium chloride 1.3 MG/ML Topical Solution	SCD	1
1049254	benzalkonium chloride 0.13 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79518-888-01	2022-01-28	C162847	48780-1	d6a99b39-b2cc-a426-e053-dadaa90af4c2	Dr. Du-More's VIRAL TERMINATOR n ano silver SKIN DISINFECTANT HAND SANITIZING
79518-888-02	2022-01-28	C162847	48780-1	d6a99b39-b2cc-a426-e053-dadaa90af4c2	Dr. Du-More's VIRAL TERMINATOR n ano silver SKIN DISINFECTANT HAND SANITIZING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79518-888-01	Dr. Du-Mores Viral Terminator Nano Silver Skin Disinfectant Hand Sanitizing	59.14 mL in 1 BOTTLE, SPRAY	LIQUID	59.14		1
79518-888-02	Dr. Du-Mores Viral Terminator Nano Silver Skin Disinfectant Hand Sanitizing	237 mL in 1 BOTTLE, SPRAY	LIQUID	237		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79518-888	DR. DU-MORES VIRAL TERMINATOR NANO SILVER SKIN DISINFECTANT HAND SANITIZING (BENZALKONIUM CHLORIDE) LIQUID [CORE PACIFIC, INC.]	1	Legacy NDC, 2 package rows	20201030_2e73e7d1-0dc9-46db-a842-17761758978a.zip

Products#

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

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

Dr. Du-Mores Viral Terminator Nano Silver Skin Disinfectant Hand Sanitizing
Benzalkonium Chloride
BENZALKONIUM
WATER
SILVER
SODIUM SESQUICARBONATE
MAGNESIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79518-888	79518-888-01, 79518-888-02

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
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
SILVER	3M4G523W1G	IACT
SODIUM SESQUICARBONATE	Y1X815621J	IACT
MAGNESIUM	I38ZP9992A	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a27be201-51d6-4190-8535-c73bc8648fa1			2e73e7d1-0dc9-46db-a842-17761758978a	2020-10-19	Warnings	Exact identifier spl id: a27be201-51d6-4190-8535-c73bc8648fa1 spl set id: 2e73e7d1-0dc9-46db-a842-17761758978a

Reported adverse events (FAERS/openFDA)#

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