Fungi Nail Toe And Foot Ointment
NDC Package 72667-346-50

11-digit billing NDC: 72667034650
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Fungi Nail Toe And Foot (tolnaftate) ointment is usesProven effective in the treatment of most athlete’s foot (tinea pedis) and ringworm (tinea corporis).Helps prevent most athlete’s foot with daily use.For effective relief of itching, burning and cracking. This formulation utilizes a ointment delivery system. Marketed by Inspec Solutions, this product is identified by NDC 72667-346 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
72667-346-50
Package Description
1 TUBE in 1 CARTON / 20 g in 1 TUBE
Product Code
72667-346
11-Digit Billing Format
72667034650

Clinical Specifications

Proprietary Name
Fungi Nail Toe And Foot
Non-Proprietary Name
Tolnaftate
Substance Name
Tolnaftate
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)
TOLNAFTATE 1 g/100g
Usage Information
UsesProven effective in the treatment of most athlete’s foot (tinea pedis) and ringworm (tinea corporis).Helps prevent most athlete’s foot with daily use.For effective relief of itching, burning and cracking.

Regulatory & Marketing

Labeler Name
Inspec Solutions
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-03-2026
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 72667-346-50 identifies a specific commercial package of 1 tube in 1 carton / 20 g in 1 tube of Fungi Nail Toe And Foot, a human over the counter drug labeled by Inspec Solutions. This ointment is formulated for topical use and contains tolnaftate 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 Inspec Solutions on November 03, 2026. The current certification is valid through December 31, 2027.

How is this Inspec Solutions product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72667034650. 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)
72667-346-50
11-Digit CMS (5-4-2)
72667-0346-50

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