Povidone Iodine Swab
NDC Package 55681-751-00

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

Package Information

Povidone Iodine swabs is tear at notch. This formulation utilizes a swab delivery system. Marketed by Twinmed Llc, this product is identified by NDC 55681-751 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
55681-751-00
Package Description
10 BOX in 1 CASE / 100 PACKET in 1 BOX / .1 g in 1 PACKET
Product Code
55681-751
11-Digit Billing Format
55681075100
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Povidone Iodine
Non-Proprietary Name
Povidone-iodine
Substance Name
Povidone-iodine
Dosage Form
Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
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 .1 g/g
Usage Information
Tear at notch. Remove applicator. Discard applicator after single use.As a first aid antispetic:Clean affected areaApply 1-3 times dailyMay be covered with a sterile bandageIf bandaged, let dry first.For preoperative patient skin preparationClean areaApply to operative site prior to surgery using applicator.

Regulatory & Marketing

Labeler Name
Twinmed Llc
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-25-2023
Listing Expiration
12-31-2026
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 55681-751-00 identifies a specific commercial package of 10 box in 1 case / 100 packet in 1 box / .1 g in 1 packet of Povidone Iodine, a human over the counter drug labeled by Twinmed Llc. This swab 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 Twinmed Llc on May 25, 2023. The current certification is valid through December 31, 2026.

How is this Twinmed Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55681075100. 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)
55681-751-00
11-Digit CMS (5-4-2)
55681-0751-00

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