Body Action Products Butt Eze Benzocaine Gel
NDC Package 70742-286-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Body Action Products Butt Eze Benzocaine (benzocaine) gel is when practial, cleanse the affected area with mild soap and warm water and rinse thoroughly.Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.Apply to the affected area up to 6 times daily. This formulation utilizes a gel delivery system. Marketed by Product Max Group Inc, this product is identified by NDC 70742-286 and is authorized under FDA application M015.

Identification & Billing

NDC Package Code
70742-286-00
Package Description
60 mL in 1 BOTTLE
Product Code
70742-286
11-Digit Billing Format
70742028600

Clinical Specifications

Proprietary Name
Body Action Products Butt Eze Benzocaine
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
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 50 mg/mL
Pharmacologic Class
Usage Information
When practial, cleanse the affected area with mild soap and warm water and rinse thoroughly.Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.Apply to the affected area up to 6 times daily.

Regulatory & Marketing

Labeler Name
Product Max Group Inc
Product Type
Human Otc Drug
FDA Application #
M015
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-29-2022
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 70742-286-00 identifies a specific commercial package of 60 ml in 1 bottle of Body Action Products Butt Eze Benzocaine, a human over the counter drug labeled by Product Max Group Inc. This gel is formulated for topical 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 Product Max Group Inc on April 29, 2022. The current certification is valid through December 31, 2026.

How is this Product Max Group Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70742028600. 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)
70742-286-00
11-Digit CMS (5-4-2)
70742-0286-00

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