NDC Package 11523-0777-2 Tinactin

Tolnaftate Aerosol, Powder 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:

11523-0777-2

Package Description:

133 g in 1 CAN

Product Code:

11523-0777

Proprietary Name:

Tinactin

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:

11523077702

Billing Unit:

GM - Billing unit of "gram" is used when a product is measured by its weight.

NDC to RxNorm Crosswalk:

133 GM

NDC to RxNorm Crosswalk:

RxCUI: 705934 - tolnaftate 1 % Powder Spray

RxCUI: 705934 - tolnaftate 0.01 MG/MG Powder Spray

RxCUI: 705936 - Tinactin 1 % Powder Spray

RxCUI: 705936 - tolnaftate 0.01 MG/MG Powder Spray [Tinactin]

RxCUI: 705936 - Tinactin 0.01 MG/MG Powder Spray

Product Type:

Human Otc Drug

Labeler Name:

Bayer Healthcare Llc.

Dosage Form:

Aerosol, Powder - A product that is packaged under pressure and contains therapeutically active ingredients, in the form of a powder, that are released upon activation of an appropriate valve system.

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/g

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:

09-23-1993

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

11523 - Bayer Healthcare Llc.
- 11523-0777 - Tinactin
  - 11523-0777-2 - 133 g in 1 CAN

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 11523-0777-2?

The NDC Packaged Code 11523-0777-2 is assigned to a package of 133 g in 1 can of Tinactin, a human over the counter drug labeled by Bayer Healthcare Llc.. The product's dosage form is aerosol, powder and is administered via topical form.

Is NDC 11523-0777 included in the NDC Directory?

Yes, Tinactin with product code 11523-0777 is active and included in the NDC Directory. The product was first marketed by Bayer Healthcare Llc. on September 23, 1993 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 11523-0777-2?

The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 133.

What is the 11-digit format for NDC 11523-0777-2?

The 11-digit format is 11523077702. 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 5-4-1 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
5-4-1	11523-0777-2	5-4-2	11523-0777-02

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