Bencocaine Topical Anesthetic Gel
NDC Package 66975-357-30

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

Package Information

Bencocaine Topical Anesthetic (benzocaine) gel is apply only amount needed to the oral mucosa to prevent or relieve pain. This formulation utilizes a gel delivery system. Marketed by Benco Dental, this product is identified by NDC 66975-357 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
66975-357-30
Package Description
30 g in 1 JAR
Product Code
11-Digit Billing Format
66975035730
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Bencocaine Topical Anesthetic
Non-Proprietary Name
Benzocaine
Substance Name
Benzocaine
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
Dental - Administration to a tooth or teeth.
Active Ingredient(s)
Usage Information
Apply only amount needed to the oral mucosa to prevent or relieve pain.

Regulatory & Marketing

Labeler Name
Benco Dental
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-27-2014
Listing Expiration
12-31-2026
Exclude Flag
N
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 66975-357-30 identifies a specific commercial package of 30 g in 1 jar of Bencocaine Topical Anesthetic, a human over the counter drug labeled by Benco Dental. This gel is formulated for dental use and contains benzocaine as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Benco Dental on June 27, 2014. The current certification is valid through December 31, 2026.

How is this Benco Dental product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 66975035730. 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)
66975-357-30
11-Digit CMS (5-4-2)
66975-0357-30

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