Providone-iodine Prep Pads
NDC Package 72766-005-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Providone-iodine Prep Pads is a . Marketed by Yangzhou Suxiang Medical Instrument Co, Ltd, this product is identified by NDC 72766-005 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
72766-005-01
Package Description
1 SWAB in 1 PACKET
Product Code
72766-005
11-Digit Billing Format
72766000501

Clinical Specifications

Proprietary Name
Providone-iodine Prep Pads
Dosage Form
-

Regulatory & Marketing

Labeler Name
Yangzhou Suxiang Medical Instrument Co, Ltd
FDA Application #
part333A
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
08-31-2022
End Marketing Date
04-25-2023
Listing Expiration
04-25-2023
Exclude Flag
D
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 72766-005-01 identifies a specific commercial package of 1 swab in 1 packet of Providone-iodine Prep Pads, labeled by Yangzhou Suxiang Medical Instrument Co, Ltd. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Yangzhou Suxiang Medical Instrument Co, Ltd on August 31, 2022. The current certification is valid through April 25, 2023.

How is this Yangzhou Suxiang Medical Instrument Co, Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72766000501. 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)
72766-005-01
11-Digit CMS (5-4-2)
72766-0005-01

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