Gingicaine Gel, Chocolate Mint
NDC Package 10129-034-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Gingicaine Gel, Chocolate Mint is a . Marketed by Gingi-pak A Division Of The Belport, this product is identified by NDC 10129-034 and is authorized under FDA application part356.

Identification & Billing

NDC Package Code
10129-034-01
Package Description
1 GEL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
10129003401
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Gingicaine Gel, Chocolate Mint
Dosage Form
-

Regulatory & Marketing

Labeler Name
Gingi-pak A Division Of The Belport
FDA Application #
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
07-06-1993
Listing Expiration
12-31-2024
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (10129-034). Click a package code to view its specific billing and regulatory data.

6 GEL in 1 BOTTLE, PLASTIC

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 10129-034-01 identifies a specific commercial package of 1 gel in 1 bottle, plastic of Gingicaine Gel, Chocolate Mint, labeled by Gingi-pak A Division Of The Belport. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Gingi-pak A Division Of The Belport on July 06, 1993. The current certification is valid through December 31, 2024.

How is this Gingi-pak A Division Of The Belport product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10129003401. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
10129-034-01
11-Digit CMS (5-4-2)
10129-0034-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.