All Day Pain Relief
NDC Package 42254-230-30
Package Information
All Day Pain Relief is do not take more than directed the smallest effective dose should be used do not take longer than 10 days, unless directed by a doctor (see Warnings) drink a full glass of water with each dose Adults and children 12 years and oldertake 1 tablet every 8 to 12 hours while symptoms last for the first dose you may take 2 tablets within the first hour do not exceed 2 tablets in any 8- to 12-hour period do not exceed 3 tablets in a 24-hour period Children under 12 years ask a doctor. Marketed by Rebel Distributors Corp, this product is identified by NDC 42254-230 and is authorized under FDA application ANDA074661.
Identification & Billing
- RxCUI: 849574 - naproxen sodium 220 MG Oral Tablet
- RxCUI: 849574 - naproxen sodium 220 MG (as naproxen 200 MG) Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 42254 - Rebel Distributors Corp
- 42254-230 - All Day Pain Relief
- 42254-230-30 - 30 TABLET in 1 BOTTLE
- 42254-230 - All Day Pain Relief
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 (42254-230). 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 42254-230-30 identifies a specific commercial package of 30 tablet in 1 bottle of All Day Pain Relief, labeled by Rebel Distributors Corp. This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package. 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 Rebel Distributors Corp on January 14, 1997. The current certification is valid through December 31, 2017.
How is this Rebel Distributors Corp product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 42254023030. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 30 total billable units per package. 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 Product segment to maintain the 5-4-2 structure.
