NDC 79781-211 Disinfectant Hand And Skin Wet Wipe

Benzalkonium Chloride

NDC Product Code 79781-211

NDC CODE: 79781-211

Proprietary Name: Disinfectant Hand And Skin Wet Wipe 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

  • 79781 - Molecule Koruyucu Saglik Urunleri Sanayi Ve Ticaret Anonim Sirketi

NDC 79781-211-01

Package Description: 5.1 g in 1 POUCH

NDC 79781-211-02

Package Description: 5.1 g in 1 POUCH

NDC Product Information

Disinfectant Hand And Skin Wet Wipe with NDC 79781-211 is a a human over the counter drug product labeled by Molecule Koruyucu Saglik Urunleri Sanayi Ve Ticaret Anonim Sirketi. The generic name of Disinfectant Hand And Skin Wet Wipe is benzalkonium chloride. The product's dosage form is swab and is administered via topical form.

Labeler Name: Molecule Koruyucu Saglik Urunleri Sanayi Ve Ticaret Anonim Sirketi

Dosage Form: Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.

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.

Disinfectant Hand And Skin Wet Wipe 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 g/100g

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)
  • ALLANTOIN (UNII: 344S277G0Z)

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: Molecule Koruyucu Saglik Urunleri Sanayi Ve Ticaret Anonim Sirketi
Labeler Code: 79781
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: 09-01-2020 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.

Disinfectant Hand And Skin Wet Wipe 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

Otc - Active Ingredient

ALKYLDIMETHYLBENZYLAMMONIUM CHLORIDE (w/w): 0,33%, purpose: antiseptic

ALCOHOL (w/w): 80%, purpose: antiseptic

Otc - Purpose



A ready to use product. On first use, open lid and remove seal label. Pull up a corner of the wipe, then carefully twist and thread it through the hole in the lid. Take as many wet wipes as you need to clean your hands and gently wipe your hands. Close the lid after use to prevent the jipes from drying out.

Indications & Usage

• For use when soap and water are not available.• Kills bacteria, viruses and fungi in 2 minute.

• Provides bactericidal, virucidal and fungicidal effect and protection against bacteria, viruses and fungi.

• Effective against gram (+) gram (-) bacteria.

• It has been shown to not cause any skin irritation.




Otc - Do Not Use

Do not use on open wounds and in children less than 2 months of age.

Otc - When Using

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water.

Otc - Stop Use

If irritation and redness develops and persist and in case of poisoning stop use and ask a doctor. Symptoms of Poisoning are dizziness, loss of consciousness and speech disorder.

Otc - Keep Out Of Reach Of Children

IF SWALLOWED : Immediately call a POISON CENTER/ doctor.

Inactive Ingredient

Aqua, Coco Glucoside, Allantoin, Citric Acid

Other Informations

Keep away from heat, sparks, open flames and hot surfaces. No smoking. Avoid release to the environment. Dispose of contents/ container in accordance with national regulations. Store between 15-30 ºC. Avoid freezing and excessive heat above 40ºC

* Please review the disclaimer below.