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  5. NDC Package Code: 0363-7998-01 Antifungal Liquid Maximum Strength

NDC Package 0363-7998-01 Antifungal Liquid Maximum Strength

Tolnaftate Liquid 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:
0363-7998-01
Package Description:
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
0363-7998
Proprietary Name:
Antifungal Liquid Maximum Strength
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:
00363799801
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:
    Walgreens Company
    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 10 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    M005
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-12-2024
    Listing Expiration Date:
    12-31-2025
    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 0363-7998-01?

    The NDC Packaged Code 0363-7998-01 is assigned to a package of 1 bottle, with applicator in 1 carton / 30 ml in 1 bottle, with applicator of Antifungal Liquid Maximum Strength, a human over the counter drug labeled by Walgreens Company. The product's dosage form is liquid and is administered via topical form.

    Is NDC 0363-7998 included in the NDC Directory?

    Yes, Antifungal Liquid Maximum Strength with product code 0363-7998 is active and included in the NDC Directory. The product was first marketed by Walgreens Company on March 12, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0363-7998-01?

    The 11-digit format is 00363799801. 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 4-4-2 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
    4-4-20363-7998-015-4-200363-7998-01