73107-105 NDC - KONIX ALCOHOL ANTISEPTIC HAND RUB ()

Drug Information

Product NDC: 73107-105

Proprietary Name: KONIX Alcohol Antiseptic Hand Rub

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	5/12/2020

No.	Package Code	Package Description
1	73107-105-30	30 mL in 1 BOTTLE (73107-105-30)
2	73107-105-31	50 mL in 1 BOTTLE (73107-105-31)
3	73107-105-32	85 mL in 1 BOTTLE (73107-105-32)
4	73107-105-33	100 mL in 1 BOTTLE (73107-105-33)
5	73107-105-34	150 mL in 1 BOTTLE (73107-105-34)
6	73107-105-35	200 mL in 1 BOTTLE (73107-105-35)
7	73107-105-36	250 mL in 1 BOTTLE (73107-105-36)
8	73107-105-37	500 mL in 1 BOTTLE (73107-105-37)
9	73107-105-38	1000 mL in 1 BOTTLE (73107-105-38)
10	73107-105-39	5000 mL in 1 BOTTLE (73107-105-39)
11	73107-105-40	5 mL in 1 PACKET (73107-105-40)

Field Name	Field Value	Definition
PRODUCT NDC	73107-105	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 Alcohol Antiseptic Hand Rub	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	5/12/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023