Mma Elite Pain Relief
NDC Package 24462-200-01

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

Package Information

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

Mma Elite Pain Relief is directions:For best results, apply generously to affected and surrounding areas. Marketed by Mma Pain Relief Gel, Llc, this product is identified by NDC 24462-200 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
24462-200-01
Package Description
2 g in 1 PACKET
Product Code
24462-200
11-Digit Billing Format
24462020001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Mma Elite Pain Relief
Dosage Form
-
Usage Information
Directions:For best results, apply generously to affected and surrounding areas. Use 1 layer for minor pain, 2 for medium and 3 layers for severs symptoms.  Rub in well.  Allow to dry between layers (usually just 2-3 minutes).  Repeat process up to 4 times daily.  For adults and children 2 years and older.  For children under 2 years of age, consult a doctor. Uses:temporary relief of minor aches and pains of musclesand joints due to:    * simple backache    * arthritis    * sprains     * strains    * bruises

Regulatory & Marketing

Labeler Name
Mma Pain Relief Gel, Llc
FDA Application #
part348
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
11-10-2011
Listing Expiration
12-31-2017
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 (24462-200). Click a package code to view its specific billing and regulatory data.

24462-200-02
88 g in 1 TUBE
24462-200-03
177 g in 1 TUBE
24462-200-04
1814 g in 1 JUG

* 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 24462-200-01 identifies a specific commercial package of 2 g in 1 packet of Mma Elite Pain Relief, labeled by Mma Pain Relief Gel, Llc. 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 Mma Pain Relief Gel, Llc on November 10, 2011. The current certification is valid through December 31, 2017.

How is this Mma Pain Relief Gel, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24462020001. 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)
24462-200-01
11-Digit CMS (5-4-2)
24462-0200-01

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