Defense Ag

Manufacturer
Nexderma Inc | Nexderma
Effective date
2020-09-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:30

Label at a glance#

ProductDefense Ag
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% - Antiseptic to help reduce bacteria that potentially can cause disease

INACTIVE INGREDIENT SECTION

Hydroxyethyl Cellulose

Curcumin

Ultra Pure Water

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Apply Defense Ag on hands rubbing together until dried. Repeat as often as necessary.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Adult super vision recommended for children under 6 years old.

Warnings

WARNINGS SECTION

Keep away from fire and flame.

Flammable

For external use on hands only

Keep out of eyes, ears and mouth.

If contact in eyes, flush thoroughly with water.

Keep out of reach of children

If swallowed seek medical help immediately or call poison control center

Store between 15-30C (58-86F)

Avoid freezing and excessive heat above 40C (104F)

Will damage wood finishes, plastics and some fabrics

Do not use

OTC - DO NOT USE SECTION

children less than 2 months of age or on open wounds.

DOSAGE & ADMINISTRATION SECTION

Dosage: upto 10 times a day

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Adminstration: Topical

OTC - PURPOSE SECTION

Purpose: to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

000 mL NDC: 00000-000-00 4oz label4oz label 8oz label8oz label 12 oz label12 oz label 16oz label16oz label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN1
1041498ethanol 0.8 ML/ML Topical GelSCD1
1041498ethanol 80 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130854804008317GTIN-13: 0854804008317
EAN-13: 0854804008317
GTIN-12: 854804008317
UPC-A: 854804008317
GTIN storage (14 digits): 00854804008317
CURCUMIN 8OZ.jpg
BarcodeEAN-130854804008324GTIN-13: 0854804008324
EAN-13: 0854804008324
GTIN-12: 854804008324
UPC-A: 854804008324
GTIN storage (14 digits): 00854804008324
curcumin 4oz.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79930-7102-1Defense Ag100 mL in 1 BOTTLE, DISPENSINGGEL1001
79930-7102-2Defense Ag250 mL in 1 BOTTLE, DISPENSINGGEL2501
79930-7102-3Defense Ag350 mL in 1 BOTTLE, DISPENSINGGEL3501
79930-7102-4Defense Ag500 mL in 1 BOTTLE, DISPENSINGGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79930-7102DEFENSE AG (DEFENSE AG SANITIZING GEL) GEL [NEXDERMA INC]1Legacy NDC, 4 package rows20200930_ae6b0c06-9ef4-7e1e-e053-2995a90a9ebb.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79930-710279930-7102-1, 79930-7102-2, 79930-7102-4, 79930-7102-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
ab3553b2-3966-4ced-e053-2a95a90a4176ae6b0c06-9ef4-7e1e-e053-2995a90a9ebb2020-09-30WarningsExact identifier
spl id: ab3553b2-3966-4ced-e053-2a95a90a4176
spl set id: ae6b0c06-9ef4-7e1e-e053-2995a90a9ebb

Reported adverse events (FAERS/openFDA)#

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