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  5. NDC Package Code: 68016-586-03 Tolnaftate

NDC Package 68016-586-03 Tolnaftate

Foot Odor Control Powder Spray Aerosol, Spray 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:
68016-586-03
Package Description:
113 g in 1 CAN
Product Code:
68016-586
Proprietary Name:
Tolnaftate
Non-Proprietary Name:
Foot Odor Control Powder Spray
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:
68016058603
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
113 GM
Product Type:
Human Otc Drug
Labeler Name:
Chain Drug Consortium, Llc
Dosage Form:
Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
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 1.3 g/113g
    • Sample Package:
    No
    FDA Application Number:
    M005
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-01-2006
    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 68016-586-03?

    The NDC Packaged Code 68016-586-03 is assigned to a package of 113 g in 1 can of Tolnaftate, a human over the counter drug labeled by Chain Drug Consortium, Llc. The product's dosage form is aerosol, spray and is administered via topical form.This product is billed per "GM" gram and contains an estimated amount of 113 billable units per package.

    Is NDC 68016-586 included in the NDC Directory?

    Yes, Tolnaftate with product code 68016-586 is active and included in the NDC Directory. The product was first marketed by Chain Drug Consortium, Llc on June 01, 2006 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 NDC billing unit for package 68016-586-03?

    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 113.

    What is the 11-digit format for NDC 68016-586-03?

    The 11-digit format is 68016058603. 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
    5-3-268016-586-035-4-268016-0586-03