Extra Strength Pain Relief
NDC Package 49738-024-26

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.

Extra Strength Pain Relief is do not take more than directed (see Overdose warning)adults and children 12 years and overtake 2 softgels every 6 hours while symptoms lastdo not take more than 6 softgels in 24 hours, unless directed by a doctordo not use for more than 10 days unless directed by a doctorchildren under 12 yearsask a doctor. Marketed by Kmart Corporation, this product is identified by NDC 49738-024 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
49738-024-26
Package Description
80 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code
49738-024
11-Digit Billing Format
49738002426
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Extra Strength Pain Relief
Dosage Form
-
Usage Information
Do not take more than directed (see Overdose warning)adults and children 12 years and overtake 2 softgels every 6 hours while symptoms lastdo not take more than 6 softgels in 24 hours, unless directed by a doctordo not use for more than 10 days unless directed by a doctorchildren under 12 yearsask a doctor

Regulatory & Marketing

Labeler Name
Kmart Corporation
FDA Application #
part343
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
06-01-2016
Listing Expiration
12-31-2024
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 (49738-024). Click a package code to view its specific billing and regulatory data.

49738-024-25
40 CAPSULE, LIQUID FILLED in 1 BOTTLE

* 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 49738-024-26 identifies a specific commercial package of 80 capsule, liquid filled in 1 bottle of Extra Strength Pain Relief, labeled by Kmart Corporation. 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 Kmart Corporation on June 01, 2016. The current certification is valid through December 31, 2024.

How is this Kmart Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49738002426. 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)
49738-024-26
11-Digit CMS (5-4-2)
49738-0024-26

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