Tm Titus Medical Povidone Iodine Ointment
NDC Package 81526-002-01

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

Package Information

Tm Titus Medical Povidone Iodine (povidone-iodine) ointment is apply locally as need. This formulation utilizes a ointment delivery system. Marketed by Titus Medical Llc, this product is identified by NDC 81526-002 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
81526-002-01
Package Description
100 POUCH in 1 BOX / 1 g in 1 POUCH
Product Code
81526-002
11-Digit Billing Format
81526000201
RxNorm Crosswalk
  • RxCUI: 312563 - povidone-iodine 10 % Topical Ointment
  • RxCUI: 312563 - povidone-iodine 0.1 MG/MG Topical Ointment
  • RxCUI: 312563 - povidone-iodine 10 % (equal to 1 % available iodine) Topical Ointment

Clinical Specifications

Proprietary Name
Tm Titus Medical Povidone Iodine
Non-Proprietary Name
Povidone-iodine
Substance Name
Povidone-iodine
Dosage Form
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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/100g
Usage Information
Apply locally as need

Regulatory & Marketing

Labeler Name
Titus Medical Llc
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-21-2021
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 81526-002-01 identifies a specific commercial package of 100 pouch in 1 box / 1 g in 1 pouch of Tm Titus Medical Povidone Iodine, a human over the counter drug labeled by Titus Medical Llc. This ointment 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 Titus Medical Llc on June 21, 2021. The current certification is valid through December 31, 2026.

How is this Titus Medical Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81526000201. 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)
81526-002-01
11-Digit CMS (5-4-2)
81526-0002-01

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