Foot Odor Control Powder Aerosol, Spray
NDC Package 56104-252-01

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

Package Information

Foot Odor Control Powder (tolnaftate) aerosols is tolnaftate is used to treat skin infections such as athlete's foot, jock itch, and ringworm. This formulation utilizes a aerosol, spray delivery system. Marketed by Premier Brands Of America Inc., this product is identified by NDC 56104-252 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
56104-252-01
Package Description
113 g in 1 CAN
Product Code
56104-252
11-Digit Billing Format
56104025201

Clinical Specifications

Proprietary Name
Foot Odor Control Powder
Non-Proprietary Name
Tolnaftate
Substance Name
Tolnaftate
Dosage Form
Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
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 1.3 g/113g
Usage Information
Tolnaftate is used to treat skin infections such as athlete's foot, jock itch, and ringworm. It is an antifungal that works by preventing the growth of fungus.

Regulatory & Marketing

Labeler Name
Premier Brands Of America Inc.
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-29-2021
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 56104-252-01 identifies a specific commercial package of 113 g in 1 can of Foot Odor Control Powder, a human over the counter drug labeled by Premier Brands Of America Inc.. This aerosol, spray 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 Premier Brands Of America Inc. on September 29, 2021. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Tolnaftate is used to treat skin infections such as athlete's foot, jock itch, and ringworm. It is an antifungal that works by preventing the growth of fungus.

How is this Premier Brands Of America Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 56104025201. 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)
56104-252-01
11-Digit CMS (5-4-2)
56104-0252-01

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