NDC 73107-108 Konix Hand Sanitizer Wipes

Konix Hand Sanitizer Wipes

NDC Product Code 73107-108

NDC 73107-108-01

Package Description: 1 SWAB in 1 PACKAGE

NDC 73107-108-20

Package Description: 20 SWAB in 1 POUCH

NDC 73107-108-40

Package Description: 40 SWAB in 1 POUCH

NDC 73107-108-75

Package Description: 75 SWAB in 1 POUCH

NDC 73107-108-76

Package Description: 175 SWAB in 1 CANISTER

NDC 73107-108-99

Package Description: 100 SWAB in 1 CANISTER

NDC Product Information

Konix Hand Sanitizer Wipes with NDC 73107-108 is a a human over the counter drug product labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler. The generic name of Konix Hand Sanitizer Wipes is konix hand sanitizer wipes. The product's dosage form is swab and is administered via topical form.

Labeler Name: Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler

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.

Konix Hand Sanitizer Wipes 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 70 mL/1

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: Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler
Labeler Code: 73107
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: 03-31-2021 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Konix Hand Sanitizer Wipes 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(S)

Ethyl Alcohol 70%




Hand sanitizer wipe  to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

For External Use Only

Flammable. Keep away from open flame and source of heat.

Do Not Use

On open skin wounds

When Using This Product

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

Stop Use And Ask A Doctor

If irritation or rash occurs.  These may be signs of serious condition.

Keep Out Of Reach Of Children.

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


Open packet. Wipe hands thoroughly with product and allow to dry. Discard wipe after use. Supervise children under 6 years of age when using this product to avoid swallowing. Do not flush.

Other Information

Store between room temperature 5-30C (41-86F). Avoid freezing and excessive heat above 40 C ( 104F).

Inactive Ingredients

Deionized water, Glycerine, Fragrance(Parfum)

Konix Hand Sanitizer Wipes

Alcohol Based Individually Wrapped 1 wipePremoistened TowelettesNDC 73107-108-01Canister

Alcohol BasedPouch20 WipesPreMoistened TowelettesNDC 73107-108-20

Alcohol BasedPouch40 WipesPreMoistened TowelettesNDC 73107-108-40

Alcohol BasedPouch75 WipesPreMoistened TowelettesNDC 73107-108-75

Alcohol BasedCanister100 WipesPreMoistened TowelettesNDC 73107-108-99

Alcohol BasedCanister175 WipesPreMoistened TowelettesNDC 73107-108-76

* Please review the disclaimer below.