Medique Back Pain Relief Tablet, Film Coated
NDC Package 47682-074-99

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

Medique Back Pain Relief (magnesium salicylate tetrahydrate) tablets is usesFor the temporary releif of minor backache pain. This formulation utilizes a tablet, film coated delivery system. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-074 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
47682-074-99
Package Description
2 TABLET, FILM COATED in 1 PACKET
Product Code
47682-074
11-Digit Billing Format
47682007499
RxNorm Crosswalk
  • RxCUI: 198742 - magnesium salicylate 580 MG Oral Tablet
  • RxCUI: 198742 - magnesium salicylate 580 MG (as magnesium salicylate anhydrous 467 MG) Oral Tablet

Clinical Specifications

Proprietary Name
Medique Back Pain Relief
Non-Proprietary Name
Magnesium Salicylate Tetrahydrate
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 releif of minor backache pain

Regulatory & Marketing

Labeler Name
Unifirst First Aid Corporation
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-26-2022
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (47682-074). Click a package code to view its specific billing and regulatory data.

47682-074-33
100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE
47682-074-36
75 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET
47682-074-80
40 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET (47682-074-99)

* 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 47682-074-99 identifies a specific commercial package of 2 tablet, film coated in 1 packet of Medique Back Pain Relief, a human over the counter drug labeled by Unifirst First Aid Corporation. 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 Unifirst First Aid Corporation on September 26, 2022. The current certification is valid through December 31, 2026.

How is this Unifirst First Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 47682007499. 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)
47682-074-99
11-Digit CMS (5-4-2)
47682-0074-99

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