Good Sense Dual Action Back Pain Tablet, Film Coated
NDC Package 0113-5299-89
Package Information
Good Sense Dual Action Back Pain (acetaminophen, ibuprofen) tablets is •do not take more than directedAdults and children 12 years and over: take 2 caplets every 8 hours while symptoms persistChildren under 12 years: ask a doctor•do not take more than 6 caplets in 24 hours, unless directed by a doctor. This formulation utilizes a tablet, film coated delivery system. Marketed by L. Perrigo Company, this product is identified by NDC 0113-5299 and is authorized under FDA application ANDA214836.
Identification & Billing
- RxCUI: 2387532 - acetaminophen 250 MG / ibuprofen 125 MG Oral Tablet
- RxCUI: 2387532 - APAP 250 MG / ibuprofen 125 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0113 - L. Perrigo Company
- 0113-5299 - Good Sense Dual Action Back Pain
- 0113-5299-89 - 1 BOTTLE in 1 CARTON / 18 TABLET, FILM COATED in 1 BOTTLE
- 0113-5299 - Good Sense Dual Action Back Pain
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.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (0113-5299). Click a package code to view its specific billing and regulatory data.
* 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 0113-5299-89 identifies a specific commercial package of 1 bottle in 1 carton / 18 tablet, film coated in 1 bottle of Good Sense Dual Action Back Pain, a human over the counter drug labeled by L. Perrigo Company. This tablet, film coated is formulated for oral use and contains acetaminophen; ibuprofen 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 L. Perrigo Company on March 07, 2024. The current certification is valid through December 31, 2026.
How is this L. Perrigo Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00113529989. 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:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.