NDC 78711-002 Antibacterial Hand Wipes Circle K

Benzalkonium Chloride (0.13%)

NDC Product Code 78711-002

NDC CODE: 78711-002

Proprietary Name: Antibacterial Hand Wipes Circle K 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 (0.13%) 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

  • 78711 - Lidersan Saglik Ve Gida Urunleri Anonim Sirketi

NDC 78711-002-60

Package Description: 60 CONTAINER in 1 CONTAINER > 1 mg in 1 CONTAINER

NDC Product Information

Antibacterial Hand Wipes Circle K with NDC 78711-002 is a a human over the counter drug product labeled by Lidersan Saglik Ve Gida Urunleri Anonim Sirketi. The generic name of Antibacterial Hand Wipes Circle K is benzalkonium chloride (0.13%). The product's dosage form is cloth and is administered via topical form.

Labeler Name: Lidersan Saglik Ve Gida Urunleri Anonim Sirketi

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It 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.

Antibacterial Hand Wipes Circle K 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.

  • BENZALKONIUM CHLORIDE .0013 mg/100mg

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)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)
  • LINALOOL, (+)- (UNII: F4VNO44C09)

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: Lidersan Saglik Ve Gida Urunleri Anonim Sirketi
Labeler Code: 78711
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: 11-01-2020 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.

Antibacterial Hand Wipes Circle K Product Label Images

Antibacterial Hand Wipes Circle K 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 Ingredients

Benalkonium chloride (0.13%)




Decrease bacteria on skin


For external use only

Do Not Use

If you are allergic to any of the ingredients

When Using This Product

Donot get into eyes.if contact occurs, rinse thoroughly with water.

Stop Use And Ask A Doctor If

Irritation or rash develops.and continues for more than 72 hours

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away


  • *adults and children 2 years and overapply to hands allow to dry without wiping*children under 2 yearsask a doctor before use 

Inactive Ingredients

Water, Phenoxyethanol, Polysorbate 20, Gycerin, PEG-7 Glyceryl Cocoate, Cocamidropropyl Betaine, Fragrance, Aloe barbadensis leaf juice, Tocopheryl Acetate, ,Disodium EDTA , Ethylparaben, Citric Acid, Citronellol,Hexyl Cinnamal,Limonene,Linalool, Ethylhexyglycerin

Adverse Reactions

Questions or comments? Visit our website at www.circlek.com

* Please review the disclaimer below.