My Pain Away
NDC Package 61500-5587-3

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

Package Information

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

My Pain Away is generously apply 3-4 times daily or more often if needed, 3 inches on and around affected area. Marketed by Topical Biomedics, Inc., this product is identified by NDC 61500-5587.

Identification & Billing

NDC Package Code
61500-5587-3
Package Description
88 mL in 1 TUBE
Product Code
61500-5587
11-Digit Billing Format
61500558703

Clinical Specifications

Proprietary Name
My Pain Away
Dosage Form
-
Usage Information
Generously apply 3-4 times daily or more often if needed, 3 inches on and around affected area. Massage in until absorbed, reapply before bedtime and in the morning. Use before and after physical activity. Apply immediately for acute trauma injuries (sprain, strain, bruise and impact injuries).

Regulatory & Marketing

Labeler Name
Topical Biomedics, Inc.
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
10-01-2014
Listing Expiration
12-31-2018
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 61500-5587-3 identifies a specific commercial package of 88 ml in 1 tube of My Pain Away, labeled by Topical Biomedics, Inc.. 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 Topical Biomedics, Inc. on October 01, 2014. The current certification is valid through December 31, 2018.

How is this Topical Biomedics, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61500558703. 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 (5-4-1)
61500-5587-3
11-Digit CMS (5-4-2)
61500-5587-03

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