Defense Ag

Manufacturer
Nederma Inc
Effective date
2020-07-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:29

Label at a glance#

ProductDefense Ag
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% - Antiseptic to help reduce bacteria that potentialy can cause disease.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerol

Carbomer

Ultra Pure Water

Uses

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 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 your 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.

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.

Administration: Topical

OTC - PURPOSE SECTION

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

Nexderma Defense Ag

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4oz label4oz label16oz 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79930-7101-12022-01-28C16284748780-1d6a99b39-fbcd-a426-e053-dadaa90af4c2aaf48a00-c5d8-2f55-e053-2a95a90aaf3d
79930-7101-42022-01-28C16284748780-1d6a99b39-fbcd-a426-e053-dadaa90af4c2aaf48a00-c5d8-2f55-e053-2a95a90aaf3d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79930-7101-1Defense Ag100 mL in 1 BOTTLEGEL1001
79930-7101-4Defense Ag500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79930-7101DEFENSE AG (DEFENSE AG HAND SANITIZING GEL) GEL [NEDERMA INC]1Legacy NDC, 2 package rows20200930_aaf48a00-c5d8-2f55-e053-2a95a90aaf3d.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
79930-710179930-7101-1, 79930-7101-4

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB

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
aaf48a00-c5d9-2f55-e053-2a95a90aaf3daaf48a00-c5d8-2f55-e053-2a95a90aaf3d2020-07-21WarningsExact identifier
spl id: aaf48a00-c5d9-2f55-e053-2a95a90aaf3d
spl set id: aaf48a00-c5d8-2f55-e053-2a95a90aaf3d

Reported adverse events (FAERS/openFDA)#

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