Back Pain Relief Tablet, Film Coated
NDC Package 84269-2550-2

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

Package Information

Back Pain Relief (magnesium salicylate) tablets is usesFor the temporary relief of minor backache pain. This formulation utilizes a tablet, film coated delivery system. Marketed by Wildman Business Group, this product is identified by NDC 84269-2550 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
84269-2550-2
Package Description
50 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET
Product Code
84269-2550
11-Digit Billing Format
84269255002
RxNorm Crosswalk
  • RxCUI: 198742 - magnesium salicylate 580 MG Oral Tablet
  • RxCUI: 198742 - magnesium salicylate 580 MG (as magnesium salicylate anhydrous 467 MG) Oral Tablet
  • RxCUI: 830388 - Doan's Extra Strength 580 MG Oral Tablet
  • RxCUI: 830388 - magnesium salicylate 580 MG Oral Tablet [Doans]
  • RxCUI: 830388 - Doan's (magnesium salicylate tetrahydrate 580 MG (equivalent to 467.2 anhydrous magnesium salicylate)) Oral Tablet

Clinical Specifications

Proprietary Name
Back Pain Relief Extra Strength Doans
Non-Proprietary Name
Magnesium Salicylate
Substance Name
Magnesium Salicylate
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
MAGNESIUM SALICYLATE 580 mg/1
Usage Information
UsesFor the temporary relief of minor backache pain

Regulatory & Marketing

Labeler Name
Wildman Business Group
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-01-2024
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 84269-2550-2 identifies a specific commercial package of 50 packet in 1 box / 2 tablet, film coated in 1 packet of Back Pain Relief Extra Strength Doans, a human over the counter drug labeled by Wildman Business Group. This tablet, film coated is formulated for oral use and contains magnesium salicylate 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 Wildman Business Group on July 01, 2024. The current certification is valid through December 31, 2026.

How is this Wildman Business Group product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84269255002. 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)
84269-2550-2
11-Digit CMS (5-4-2)
84269-2550-02

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