NDC Package 49406-004-75 Fungifoam

Tolnaftate Aerosol, Foam Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

49406-004-75

Package Description:

1 BOTTLE in 1 BOX / 75 mL in 1 BOTTLE

Product Code:

49406-004

Proprietary Name:

Fungifoam

Non-Proprietary Name:

Tolnaftate

Substance Name:

Tolnaftate

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.

11-Digit NDC Billing Format:

49406000475

NDC to RxNorm Crosswalk:

RxCUI: 1356533 - tolnaftate 1 % Topical Foam

RxCUI: 1356533 - tolnaftate 10 MG/ML Topical Foam

RxCUI: 1356538 - FungiFoam 1 % Topical Foam

RxCUI: 1356538 - tolnaftate 10 MG/ML Topical Foam [Fungifoam]

RxCUI: 1356538 - Fungifoam 10 MG/ML Topical Foam

Product Type:

Human Otc Drug

Labeler Name:

The Tetra Corporation

Dosage Form:

Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.

Administration Route(s):

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 10 mg/mL

Sample Package:

FDA Application Number:

M005

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

07-13-2020

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

49406 - The Tetra Corporation
- 49406-004 - Fungifoam
  - 49406-004-75 - 1 BOTTLE in 1 BOX / 75 mL in 1 BOTTLE

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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
49406-004-30	1 TUBE in 1 BOX / 30 mL in 1 TUBE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 49406-004-75?

The NDC Packaged Code 49406-004-75 is assigned to a package of 1 bottle in 1 box / 75 ml in 1 bottle of Fungifoam, a human over the counter drug labeled by The Tetra Corporation. The product's dosage form is aerosol, foam and is administered via topical form.

Is NDC 49406-004 included in the NDC Directory?

Yes, Fungifoam with product code 49406-004 is active and included in the NDC Directory. The product was first marketed by The Tetra Corporation on July 13, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 49406-004-75?

The 11-digit format is 49406000475. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	49406-004-75	5-4-2	49406-0004-75

Table of Contents