NDC Package 10129-063-03 Gingicaine Gel, Mint Julep

Gingicaine Gel,Mint Julep Flabvor Gel Dental; Oral; Periodontal - View Billable Units, 11-Digit Format, RxNorm

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:
10129-063-03
Package Description:
1 GEL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Gingicaine Gel, Mint Julep
Non-Proprietary Name:
Gingicaine Gel, Mint Julep Flabvor
Substance Name:
Benzocaine
11-Digit NDC Billing Format:
10129006303
NDC to RxNorm Crosswalk:
  • RxCUI: 238910 - benzocaine 20 % Oral Gel
  • RxCUI: 238910 - benzocaine 0.2 MG/MG Oral Gel
  • RxCUI: 238910 - benzocaine 20 % (180-220 MG per 1 GM) Oral Gel
  • RxCUI: 543801 - Gingicaine 20 % Oral Gel
  • RxCUI: 543801 - benzocaine 0.2 MG/MG Oral Gel [Gingicaine]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Gingi-pak A Division Of The Belport
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
  • Oral - Administration to or by way of the mouth.
  • Periodontal - Administration around a tooth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    07-13-1998
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    10129-063-056 GEL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 10129-063-03?

    The NDC Packaged Code 10129-063-03 is assigned to a package of 1 gel in 1 bottle, plastic of Gingicaine Gel, Mint Julep, a human over the counter drug labeled by Gingi-pak A Division Of The Belport. The product's dosage form is gel and is administered via dental; oral; periodontal form.

    Is NDC 10129-063 included in the NDC Directory?

    Yes, Gingicaine Gel, Mint Julep with product code 10129-063 is active and included in the NDC Directory. The product was first marketed by Gingi-pak A Division Of The Belport on July 13, 1998 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 10129-063-03?

    The 11-digit format is 10129006303. 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
    5-3-210129-063-035-4-210129-0063-03