NDC 73107-106 Konix Hand Sanitizer Gel

Konix Hand Sanitizer Gel

NDC Product Code 73107-106

NDC 73107-106-10

Package Description: 30 mL in 1 BOTTLE

NDC 73107-106-11

Package Description: 50 mL in 1 BOTTLE

NDC 73107-106-12

Package Description: 85 mL in 1 BOTTLE

NDC 73107-106-13

Package Description: 100 mL in 1 BOTTLE

NDC 73107-106-14

Package Description: 150 mL in 1 BOTTLE

NDC 73107-106-15

Package Description: 200 mL in 1 BOTTLE

NDC 73107-106-16

Package Description: 250 mL in 1 BOTTLE

NDC 73107-106-17

Package Description: 500 mL in 1 BOTTLE

NDC 73107-106-18

Package Description: 1000 mL in 1 BOTTLE

NDC 73107-106-19

Package Description: 5000 mL in 1 BOTTLE

NDC 73107-106-40

Package Description: 5 mL in 1 PACKET

NDC 73107-106-41

Package Description: 59 mL in 1 BOTTLE

NDC 73107-106-42

Package Description: 118 mL in 1 BOTTLE

NDC 73107-106-43

Package Description: 236 mL in 1 BOTTLE

NDC 73107-106-44

Package Description: 354 mL in 1 BOTTLE

NDC 73107-106-45

Package Description: 473 mL in 1 BOTTLE

NDC 73107-106-46

Package Description: 591 mL in 1 BOTTLE

NDC 73107-106-47

Package Description: 710 mL in 1 BOTTLE

NDC 73107-106-48

Package Description: 946 mL in 1 BOTTLE

NDC 73107-106-49

Package Description: 3780 mL in 1 BOTTLE

NDC Product Information

Konix Hand Sanitizer Gel with NDC 73107-106 is a a human over the counter drug product labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As. The generic name of Konix Hand Sanitizer Gel is konix hand sanitizer gel. The product's dosage form is gel and is administered via topical form.

Labeler Name: Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As

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.

Konix Hand Sanitizer Gel 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/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.

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

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: Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As
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: 07-03-2020 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.

Konix Hand Sanitizer Gel 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 70%


Antiseptic, Hand Sanitizer Gel


To decrease bacteria on the skin that could cause disease


For external use only: hands.Flammable, keep away from fire or flame.

Otc - When Using

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin do not inhale or ingest

Otc - Stop Use

Stop use and ask a doctor if Irritation and redness develop Condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.


Wet hands thoroughly with product and allow to dry without wiping for children under 6 year of age, use only under adult supervision Not recommended for infants

Other Information

Do not store above 105°Fmay discolor some fabricsharmful to wood finishes and plastics

Inactive Ingredients

Water, Glycerin, Carbomer, Fragrance, Aminomethyl Propanol

* Please review the disclaimer below.