NDC Package 59088-477-03 Micotrin Al

Tolnaftate Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

59088-477-03

Package Description:

30 mL in 1 BOTTLE, WITH APPLICATOR

Product Code:

59088-477

Proprietary Name:

Micotrin Al

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:

59088047703

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

30 ML

NDC to RxNorm Crosswalk:

RxCUI: 313423 - tolnaftate 1 % Topical Solution

RxCUI: 313423 - tolnaftate 10 MG/ML Topical Solution

Product Type:

Human Otc Drug

Labeler Name:

Puretek Corporation

Dosage Form:

Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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 .3 g/30mL

Sample Package:

FDA Application Number:

part333C

Marketing Category:

OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.

Start Marketing Date:

10-25-2021

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

59088 - Puretek Corporation
- 59088-477 - Micotrin Al
  - 59088-477-03 - 30 mL in 1 BOTTLE, WITH APPLICATOR

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.

Frequently Asked Questions

What is NDC 59088-477-03?

The NDC Packaged Code 59088-477-03 is assigned to a package of 30 ml in 1 bottle, with applicator of Micotrin Al, a human over the counter drug labeled by Puretek Corporation. The product's dosage form is liquid and is administered via topical form.This product is billed per "ML" milliliter and contains an estimated amount of 30 billable units per package.

Is NDC 59088-477 included in the NDC Directory?

Yes, Micotrin Al with product code 59088-477 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on October 25, 2021 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 NDC billing unit for package 59088-477-03?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 30.

What is the 11-digit format for NDC 59088-477-03?

The 11-digit format is 59088047703. 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	59088-477-03	5-4-2	59088-0477-03

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