Konix Hand Sanitizer Gel

Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As
Human Otc Drug
NDC 73107-106

Konix Hand Sanitizer Gel is a human otc drug labeled by 'Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As'. National Drug Code (NDC) number for Konix Hand Sanitizer Gel is 73107-106. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Konix Hand Sanitizer Gel drug includes Alcohol - 70 mL/100mL . The currest status of Konix Hand Sanitizer Gel drug is Active.

Drug Information:

Drug NDC:	73107-106
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Konix Hand Sanitizer Gel
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Konix Hand Sanitizer Gel
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Gel
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ALCOHOL - 70 mL/100mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	OTC MONOGRAPH NOT FINAL
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	03 Jul, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number:	part333A
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:	581662
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	8683229602488 8681715345543 8681715345598 8681715345512 8681715345574 8681715345550 8681715345567 8681715345581 8681715345529 8681715345536 8681715345611
UPC stands for Universal Product Code.
UNII:	3K9958V90M
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
73107-106-10	30 mL in 1 BOTTLE (73107-106-10)	03 Jul, 2020	N/A	No
73107-106-11	50 mL in 1 BOTTLE (73107-106-11)	03 Jul, 2020	N/A	No
73107-106-12	85 mL in 1 BOTTLE (73107-106-12)	03 Jul, 2020	N/A	No
73107-106-13	100 mL in 1 BOTTLE (73107-106-13)	03 Jul, 2020	N/A	No
73107-106-14	150 mL in 1 BOTTLE (73107-106-14)	03 Jul, 2020	N/A	No
73107-106-15	200 mL in 1 BOTTLE (73107-106-15)	03 Jul, 2020	N/A	No
73107-106-16	250 mL in 1 BOTTLE (73107-106-16)	03 Jul, 2020	N/A	No
73107-106-17	500 mL in 1 BOTTLE (73107-106-17)	03 Jul, 2020	N/A	No
73107-106-18	1000 mL in 1 BOTTLE (73107-106-18)	03 Jul, 2020	N/A	No
73107-106-19	5000 mL in 1 BOTTLE (73107-106-19)	03 Jul, 2020	N/A	No
73107-106-20	20 mL in 1 PACKET (73107-106-20)	24 May, 2022	N/A	No
73107-106-40	5 mL in 1 PACKET (73107-106-40)	03 Jul, 2020	N/A	No
73107-106-41	59 mL in 1 BOTTLE (73107-106-41)	03 Jul, 2020	N/A	No
73107-106-42	118 mL in 1 BOTTLE (73107-106-42)	03 Jul, 2020	N/A	No
73107-106-43	236 mL in 1 BOTTLE (73107-106-43)	03 Jul, 2020	N/A	No
73107-106-44	354 mL in 1 BOTTLE (73107-106-44)	03 Jul, 2020	N/A	No
73107-106-45	473 mL in 1 BOTTLE (73107-106-45)	03 Jul, 2020	N/A	No
73107-106-46	591 mL in 1 BOTTLE (73107-106-46)	03 Jul, 2020	N/A	No
73107-106-47	710 mL in 1 BOTTLE (73107-106-47)	03 Jul, 2020	N/A	No
73107-106-48	946 mL in 1 BOTTLE (73107-106-48)	03 Jul, 2020	N/A	No
73107-106-49	3780 mL in 1 BOTTLE (73107-106-49)	03 Jul, 2020	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Konix Hand Sanitizer Gel

Gel
Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS
NDC: 73107-106

Purpose:

Purpose antiseptic, hand sanitizer gel

Product Elements:

Konix hand sanitizer gel konix hand sanitizer gel alcohol alcohol water glycerin carbomer 940 aminomethylpropanol

Indications and Usage:

Use to decrease bacteria on the skin that could cause disease

Warnings:

Warnings for external use only: hands. flammable, keep away from fire or flame.

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

Dosage and Administration:

Directions 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

Stop Use:

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

Package Label Principal Display Panel:

Konix hand sanitizer gel 30 ml konix %70 hand sanitizer gel 30 ml

Konix sanitizer gel 5ml konix %70 hand sanitizer gel 5 ml

Konix sanitizer gel 50 ml konix %70 hand sanitizer gel 50 ml

Konix sanitizer gel 85 ml konix 85 ml

Konix sanitizer gel 150 ml konix 150 ml

Konix sanitizer gel 200 ml konix 200 ml

Konix sanitizer gel 250 ml konix 250 ml

Konix sanitizer gel 1000 ml konix 1000 ml

Konix sanitizer gel 5000 ml konix 5000 ml

Konix sanitizer gel 100 ml konix 100 ml

Konix sanitizer gel 500 ml konix 500 ml

Konix sanitizer gel 2fl oz 59 ml konix 2fl oz 59 ml

Konix sanitizer gel 4fl oz 118 ml konix 4 fl oz. 118 ml

Konix sanitizer gel 8 fl oz. 236ml konix 8 fl oz. 236 ml

Konix sanitizer gel 12 fl oz. 354 ml konix 12 fl oz. 354 ml

Konix sanitizer gel 16 fl oz. 473 ml konix 16 fl oz. 473 ml

Konix sanitizer gel 20 fl oz. 591ml. konix 20 fl oz. 591 ml

Konix sanitizer gel 32 fl oz. 946ml konix 32 fl oz 946 ml

Konix sanitizer gel 24 fl oz. 710 ml konix 24 fl oz. 710 ml

Konix sanitizer gel 1 gal 3.78l konix 1 gal 3.78 l.

Konix sanitizer gel 20ml 0.68 oz konix hand sanitizer topical gel 20 ml sachet

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.