NDC 81499-002 Ecoshield Skin Advanced Antimicrobial Hand Sanitizer

Benzalkonium Chloride

NDC Product Code 81499-002

NDC CODE: 81499-002

Proprietary Name: Ecoshield Skin Advanced Antimicrobial Hand Sanitizer What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Benzalkonium Chloride What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 81499 - Matrix Antimicrobial, Llc

NDC 81499-002-01

Package Description: 1000 mL in 1 POUCH

NDC 81499-002-02

Package Description: 3780 mL in 1 BOTTLE

NDC Product Information

Ecoshield Skin Advanced Antimicrobial Hand Sanitizer with NDC 81499-002 is a a human over the counter drug product labeled by Matrix Antimicrobial, Llc. The generic name of Ecoshield Skin Advanced Antimicrobial Hand Sanitizer is benzalkonium chloride. The product's dosage form is solution and is administered via topical form.

Labeler Name: Matrix Antimicrobial, Llc

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.

Ecoshield Skin Advanced Antimicrobial Hand Sanitizer 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.


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.

  • 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.

Product Labeler Information

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

Labeler Name: Matrix Antimicrobial, Llc
Labeler Code: 81499
FDA Application Number: part333E 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: 02-01-2021 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: 12-31-2022 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.

Ecoshield Skin Advanced Antimicrobial Hand Sanitizer Product Label Images

Ecoshield Skin Advanced Antimicrobial Hand Sanitizer 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

Benzalkonium Chloride 0.13%


Antimicrobial Hand Sanitizer


  • Hand sanitizer to help kill 99.9% of germs.Recommended for repeated use.


For external use only.

Do Not Use

  • In ears or mouth and avoid mucus membranes.

When Using This Product.

  • Avoid contact with the eyes.In case of contact flush eyes with water.

Stop Use And Ask A Doctor If

Redness or irritation develop and persist for more than 72 hours.

Keep Out Of Reach Of Children.

Children should be supervised when using this product.


  • Apply a small amount into palms of hands and spread on both hands.Rub into skin until dry.To maintain maximum effectiveness, apply to clean dry hands every 6 to 8 hours.

Inactive Ingredients

Water, 3-(Trimethoxy) Propyl Dimethyl Octadecyl Ammonium Chloride, ethoxylated alcohol, Citrus Limon (Lemon) Fruit Oil.

* Please review the disclaimer below.