NDC 73107-109 Konix Hand Antiseptic

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:
73107-109
Proprietary Name:
Konix Hand Antiseptic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler
Labeler Code:
73107
Start Marketing Date: [9]
01-27-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 73107-109-42

Package Description: 113 g in 1 BOTTLE, SPRAY

NDC Code 73107-109-50

Package Description: 142 g in 1 BOTTLE, SPRAY

NDC Code 73107-109-51

Package Description: 170 g in 1 BOTTLE, SPRAY

NDC Code 73107-109-52

Package Description: 283.5 g in 1 BOTTLE, SPRAY

NDC Code 73107-109-53

Package Description: 350.4 g in 1 BOTTLE, SPRAY

NDC Code 73107-109-54

Package Description: 425.24 g in 1 BOTTLE, SPRAY

Product Details

What is NDC 73107-109?

The NDC code 73107-109 is assigned by the FDA to the product Konix Hand Antiseptic which is product labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 73107-109-42 113 g in 1 bottle, spray , 73107-109-50 142 g in 1 bottle, spray , 73107-109-51 170 g in 1 bottle, spray , 73107-109-52 283.5 g in 1 bottle, spray , 73107-109-53 350.4 g in 1 bottle, spray , 73107-109-54 425.24 g in 1 bottle, spray . 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 Antiseptic?

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.

Which are Konix Hand Antiseptic UNII Codes?

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

Which are Konix Hand Antiseptic 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 Antiseptic?

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".