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  5. NDC Package Code: 10129-071-01 Ultracare Anesthetic Gel

NDC Package 10129-071-01 Ultracare Anesthetic Gel

Benzocaine Gel Dental; Periodontal; 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:
10129-071-01
Package Description:
30 g in 1 BOTTLE
Product Code:
10129-071
Proprietary Name:
Ultracare Anesthetic Gel
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Anesthesia of mucous membrane of oropharynx. Minimizes the pain of ulcers, needle puncture, deep scaling procedures, and the application of matrix bands. Also an aid in the taking of impressions or intraoral radiographs of patients with an excessive gag reflexes.
11-Digit NDC Billing Format:
10129007101
Billing Unit:
C73365
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
The Bellport Company, Inc. Dba Gingi-pak
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.
  • Periodontal - Administration around a tooth.
  • 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):
BENZOCAINE 200 mg/g
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M022
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
02-08-2023
Listing Expiration Date:
12-31-2026
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 10129-071-01?

The NDC Packaged Code 10129-071-01 is assigned to a package of 30 g in 1 bottle of Ultracare Anesthetic Gel, a human over the counter drug labeled by The Bellport Company, Inc. Dba Gingi-pak. The product's dosage form is gel and is administered via dental; periodontal; topical form.

Is NDC 10129-071 included in the NDC Directory?

Yes, Ultracare Anesthetic Gel with product code 10129-071 is active and included in the NDC Directory. The product was first marketed by The Bellport Company, Inc. Dba Gingi-pak on February 08, 2023 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 10129-071-01?

The contents of this package are billed C73365

What is the 11-digit format for NDC 10129-071-01?

The 11-digit format is 10129007101. 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
5-3-210129-071-015-4-210129-0071-01