Fungi Nail Toe And Foot Solution
NDC Package 55505-177-80

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

Package Information

Fungi Nail Toe And Foot (tolnaftate) solution is tolnaftate is used to treat skin infections such as athlete's foot, jock itch, and ringworm. This formulation utilizes a solution delivery system. Marketed by Kramer Laboratories, this product is identified by NDC 55505-177 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
55505-177-80
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY
Product Code
55505-177
11-Digit Billing Format
55505017780
RxNorm Crosswalk
  • RxCUI: 2120579 - FUNGI-NAIL 1 % Topical Solution, Reformulated Mar 2019
  • RxCUI: 2120579 - tolnaftate 10 MG/ML Topical Solution [Fungi-Nail Reformulated Mar 2019]
  • RxCUI: 2120579 - Fungi-Nail Reformulated Mar 2019 1 % Topical Solution
  • RxCUI: 2120579 - Fungi-Nail Reformulated Mar 2019 10 MG/ML Topical Solution
  • RxCUI: 313423 - tolnaftate 1 % Topical Solution

Clinical Specifications

Proprietary Name
Fungi Nail Toe And Foot
Non-Proprietary Name
Tolnaftate
Substance Name
Tolnaftate
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible 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 10 mg/mL
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
Kramer Laboratories
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-25-2019
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (55505-177). Click a package code to view its specific billing and regulatory data.

55505-177-24
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 15 mL in 1 BOTTLE, WITH APPLICATOR
55505-177-26
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR
55505-177-87
2 CARTON in 1 PACKAGE / 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR

* 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 55505-177-80 identifies a specific commercial package of 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray of Fungi Nail Toe And Foot, a human over the counter drug labeled by Kramer Laboratories. This solution 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 Kramer Laboratories on March 25, 2019. 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 Kramer Laboratories product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55505017780. 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)
55505-177-80
11-Digit CMS (5-4-2)
55505-0177-80

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