NDC 79930-7101 Defense Ag

Defense Ag Hand Sanitizing Gel

NDC Product Code 79930-7101

NDC 79930-7101-1

Package Description: 100 mL in 1 BOTTLE

NDC 79930-7101-4

Package Description: 500 mL in 1 BOTTLE

NDC Product Information

Defense Ag with NDC 79930-7101 is a a human over the counter drug product labeled by Nederma Inc. The generic name of Defense Ag is defense ag hand sanitizing gel. The product's dosage form is gel and is administered via topical form.

Labeler Name: Nederma Inc

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Defense Ag Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 80 mL/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • CARBOMER 940 (UNII: 4Q93RCW27E)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nederma Inc
Labeler Code: 79930
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-30-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Defense Ag Product Label Images

Defense Ag Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

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

Inactive Ingredients

GlycerolCarbomerUltra Pure Water


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

Adult super vision recommended for children under 6 years old.


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

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

Dosage & Administration

Dosage: upto 10 times a dayPlace enough product on hands to cover all surfaces. Rub hands together until dry. Administration: Topical

Otc - Purpose

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

* Please review the disclaimer below.