NDC 73107-106 Konix Hand Sanitizer Gel

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73107-106
Proprietary Name:
Konix Hand Sanitizer Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As
Labeler Code:
73107
Start Marketing Date: [9]
07-03-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 73107-106-10

Package Description: 30 mL in 1 BOTTLE

NDC Code 73107-106-11

Package Description: 50 mL in 1 BOTTLE

NDC Code 73107-106-12

Package Description: 85 mL in 1 BOTTLE

NDC Code 73107-106-13

Package Description: 100 mL in 1 BOTTLE

NDC Code 73107-106-14

Package Description: 150 mL in 1 BOTTLE

NDC Code 73107-106-15

Package Description: 200 mL in 1 BOTTLE

NDC Code 73107-106-16

Package Description: 250 mL in 1 BOTTLE

NDC Code 73107-106-17

Package Description: 500 mL in 1 BOTTLE

NDC Code 73107-106-18

Package Description: 1000 mL in 1 BOTTLE

NDC Code 73107-106-19

Package Description: 5000 mL in 1 BOTTLE

NDC Code 73107-106-20

Package Description: 20 mL in 1 PACKET

NDC Code 73107-106-40

Package Description: 5 mL in 1 PACKET

NDC Code 73107-106-41

Package Description: 59 mL in 1 BOTTLE

NDC Code 73107-106-42

Package Description: 118 mL in 1 BOTTLE

NDC Code 73107-106-43

Package Description: 236 mL in 1 BOTTLE

NDC Code 73107-106-44

Package Description: 354 mL in 1 BOTTLE

NDC Code 73107-106-45

Package Description: 473 mL in 1 BOTTLE

NDC Code 73107-106-46

Package Description: 591 mL in 1 BOTTLE

NDC Code 73107-106-47

Package Description: 710 mL in 1 BOTTLE

NDC Code 73107-106-48

Package Description: 946 mL in 1 BOTTLE

NDC Code 73107-106-49

Package Description: 3780 mL in 1 BOTTLE

Product Details

What is NDC 73107-106?

The NDC code 73107-106 is assigned by the FDA to the product Konix Hand Sanitizer Gel which is product labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As. The product's dosage form is . The product is distributed in 21 packages with assigned NDC codes 73107-106-10 30 ml in 1 bottle , 73107-106-11 50 ml in 1 bottle , 73107-106-12 85 ml in 1 bottle , 73107-106-13 100 ml in 1 bottle , 73107-106-14 150 ml in 1 bottle , 73107-106-15 200 ml in 1 bottle , 73107-106-16 250 ml in 1 bottle , 73107-106-17 500 ml in 1 bottle , 73107-106-18 1000 ml in 1 bottle , 73107-106-19 5000 ml in 1 bottle , 73107-106-20 20 ml in 1 packet , 73107-106-40 5 ml in 1 packet , 73107-106-41 59 ml in 1 bottle , 73107-106-42 118 ml in 1 bottle , 73107-106-43 236 ml in 1 bottle , 73107-106-44 354 ml in 1 bottle , 73107-106-45 473 ml in 1 bottle , 73107-106-46 591 ml in 1 bottle , 73107-106-47 710 ml in 1 bottle , 73107-106-48 946 ml in 1 bottle , 73107-106-49 3780 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Konix Hand Sanitizer Gel?

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

Which are Konix Hand Sanitizer Gel UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Konix Hand Sanitizer Gel Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Konix Hand Sanitizer Gel?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".