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  5. NDC Package Code: 83767-501-02 Fungal Nail Treatment Maximum Strength Liquid

NDC Package 83767-501-02 Fungal Nail Treatment Maximum Strength Liquid

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
83767-501-02
Package Description:
4 BOTTLE in 1 PACKAGE / 30 mL in 1 BOTTLE
Product Code:
83767-501
Proprietary Name:
Fungal Nail Treatment Maximum Strength Liquid
Non-Proprietary Name:
Tolnaftate
Substance Name:
Tolnaftate; Undecylenic Acid
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:
83767050102
NDC to RxNorm Crosswalk:
  • RxCUI: 2691548 - tolnaftate 1 % / undecylenic acid 25 % Topical Solution
  • RxCUI: 2691548 - tolnaftate 10 MG/ML / undecylenic acid 250 MG/ML Topical Solution
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Ruijiu Electronic Technology Co., Ltd.
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):
Sample Package:
No
FDA Application Number:
M005
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-28-2024
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
83767-501-012 BOTTLE in 1 PACKAGE / 30 mL in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 83767-501-02?

The NDC Packaged Code 83767-501-02 is assigned to a package of 4 bottle in 1 package / 30 ml in 1 bottle of Fungal Nail Treatment Maximum Strength Liquid, a human over the counter drug labeled by Guangzhou Ruijiu Electronic Technology Co., Ltd.. The product's dosage form is liquid and is administered via topical form.

Is NDC 83767-501 included in the NDC Directory?

Yes, Fungal Nail Treatment Maximum Strength Liquid with product code 83767-501 is active and included in the NDC Directory. The product was first marketed by Guangzhou Ruijiu Electronic Technology Co., Ltd. on August 28, 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 83767-501-02?

The 11-digit format is 83767050102. 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
5-3-283767-501-025-4-283767-0501-02