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  5. NDC Package Code: 81929-001-01 Derman Antifungal Powder Tolnaftate

NDC Package 81929-001-01 Derman Antifungal Powder Tolnaftate

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

Table of Contents

    1. Package Information
    2. 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:
81929-001-01
Package Description:
1 CAN in 1 BOX / 130 g in 1 CAN
Product Code:
81929-001
Proprietary Name:
Derman Antifungal Powder Tolnaftate
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:
81929000101
NDC to RxNorm Crosswalk:
  • RxCUI: 705934 - tolnaftate 1 % Powder Spray
  • RxCUI: 705934 - tolnaftate 0.01 MG/MG Powder Spray
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Taisho Pharmaceutical California Inc.
    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:
    No
    FDA Application Number:
    M005
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-01-2022
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 81929-001-01?

    The NDC Packaged Code 81929-001-01 is assigned to a package of 1 can in 1 box / 130 g in 1 can of Derman Antifungal Powder Tolnaftate, a human over the counter drug labeled by Taisho Pharmaceutical California Inc.. The product's dosage form is aerosol, powder and is administered via topical form.

    Is NDC 81929-001 included in the NDC Directory?

    Yes, Derman Antifungal Powder Tolnaftate with product code 81929-001 is active and included in the NDC Directory. The product was first marketed by Taisho Pharmaceutical California Inc. on May 01, 2022 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 81929-001-01?

    The 11-digit format is 81929000101. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-281929-001-015-4-281929-0001-01