Konix Povidone Iodine Topical Antiseptic Liquid
NDC Package 73107-009-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Konix Povidone Iodine Topical Antiseptic (povidone-iodine) liquids is patient Preperative Skin Preparation: Clean the area. This formulation utilizes a liquid delivery system. Marketed by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Ticaret As, this product is identified by NDC 73107-009 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
73107-009-01
Package Description
120 mL in 1 BOTTLE
Product Code
73107-009
11-Digit Billing Format
73107000901
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Konix Povidone Iodine Topical Antiseptic
Non-Proprietary Name
Povidone-iodine
Substance Name
Povidone-iodine
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
POVIDONE-IODINE 100 mg/mL
Usage Information
Patient Preperative Skin Preparation: Clean the area. Apply product to the operative site prior to sugery.First Aid:Clean the affected area. Apply a small amount of this product on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first. 

Regulatory & Marketing

Labeler Name
Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Ticaret As
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-18-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 73107-009-01 identifies a specific commercial package of 120 ml in 1 bottle of Konix Povidone Iodine Topical Antiseptic, a human over the counter drug labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Ticaret As. This liquid is formulated for topical use and contains povidone-iodine as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Ticaret As on August 18, 2025. The current certification is valid through December 31, 2027.

How is this Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Ticaret As product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73107000901. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
73107-009-01
11-Digit CMS (5-4-2)
73107-0009-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.