NDC 73107-109 Konix Hand Antiseptic

Konix Hand Antiseptic Spray

  1. Labeler Index
  2. Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler
  3. NDC: 73107-109 Konix Hand Antiseptic

NDC Product Code 73107-109

NDC CODE: 73107-109

Proprietary Name: Konix Hand Antiseptic 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: Konix Hand Antiseptic Spray 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

NDC 73107-109-42

Package Description: 113 g in 1 BOTTLE, SPRAY

NDC 73107-109-50

Package Description: 142 g in 1 BOTTLE, SPRAY

NDC 73107-109-51

Package Description: 170 g in 1 BOTTLE, SPRAY

NDC 73107-109-52

Package Description: 283.5 g in 1 BOTTLE, SPRAY

NDC 73107-109-53

Package Description: 350.4 g in 1 BOTTLE, SPRAY

NDC 73107-109-54

Package Description: 425.24 g in 1 BOTTLE, SPRAY

NDC Product Information

Konix Hand Antiseptic with NDC 73107-109 is a a human over the counter drug product labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler. The generic name of Konix Hand Antiseptic is konix hand antiseptic spray. The product's dosage form is aerosol, spray and is administered via topical form.

Labeler Name: Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler

Dosage Form: Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous 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.

Konix Hand Antiseptic 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 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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • NITROGEN (UNII: N762921K75)

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: 01-27-2021 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.

Konix Hand Antiseptic Product Label Images

Konix Hand Antiseptic 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%

Purpose

Antiseptic

Use

Hand sanitizer recommended for repeated useto 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. Contents under pressure. Do not place in hot water or near radiators, stoves or other sources of heat.

Do Not Use

On open skin wounds

When Using This Product

Do not puncture or incinerate container. Do not inhale or ingest. Keep out of eyes, ears and mouth. If contact occurs, rinse thoroughly with water.

Stop Use And Ask A Doctor

If irritation develops

Keep Out Of Reach Of Children.

If swallowed,  call a Poison Control Center right away

Directions

Spray enough product on hands to cover all surfaces. Spray from a distance of 4 inches (10cm) for general use. Rub hands together for 30 seconds until they feel dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

Store at room temperature 5-30C (41-86F). Avoid freezing and excessive heat above 40 C ( 104F). Do not reuse container. Dispose of properly.

Inactive Ingredients

Water (aqua), Glycerine, Nitrogen (as propellant), Fragrance(Parfum)

Konix Hand Antiseptic

Continuous SprayScented70% Alcoholwiht MoisturizerNet 4OZ (113g)

Continuous SprayScented70% Alcoholwith MoisturizerNet 5 OZ  (142g)

Continuous SprayScented70% Alcoholwith MoisturizerNet 6 OZ (170g)

Continuous SprayScented70% Alcoholwith MoisturizerNet 10 Oz  (283.5g)

Continuous SprayScented70% Alcoholwith MoisturizerNet 12.5OZ (350.4g)

Continuous SprayScented70% Alcoholwith MoisturizerNet 15 OZ (425.24g)

* Please review the disclaimer below.