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  5. NDC Package Code: 83462-002-01 Tobcharm

NDC Package 83462-002-01 Tobcharm

Undecylenic Acid 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:
83462-002-01
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
83462-002
Proprietary Name:
Tobcharm
Non-Proprietary Name:
Undecylenic Acid
Substance Name:
Undecylenic Acid
Usage Information:
Wash feet thoroughly with warm water, and gently file thickened part of the fungal nail with a nail file until its flatapply layer of the liquid to the surface of the fungal nail and allow it to be absorbed into the nail. after the liquid has been absorbed, apply a layer of the cream to the infected parts of the nail repeat the process if necessary once a day  
11-Digit NDC Billing Format:
83462000201
NDC to RxNorm Crosswalk:
  • RxCUI: 1251008 - undecylenic acid 10 % Topical Solution
  • RxCUI: 1251008 - undecylenic acid 100 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Eubizrival Llc
    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):
  • UNDECYLENIC ACID 10 g/100mL
    • Sample Package:
    No
    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:
    09-05-2023
    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 83462-002-01?

    The NDC Packaged Code 83462-002-01 is assigned to a package of 30 ml in 1 bottle, glass of Tobcharm, a human over the counter drug labeled by Eubizrival Llc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 83462-002 included in the NDC Directory?

    Yes, Tobcharm with product code 83462-002 is active and included in the NDC Directory. The product was first marketed by Eubizrival Llc on September 05, 2023 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 83462-002-01?

    The 11-digit format is 83462000201. 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
    5-3-283462-002-015-4-283462-0002-01