Valumeds Pain Relief Pm Pain Reliever And Nighttime Sleep Aid Acetaminophen, Extra Strength Tablet
NDC Package 82725-1024-1
Package Information
Valumeds Pain Relief Pm Pain Reliever And Nighttime Sleep Aid Acetaminophen, Extra Strength (acetaminophen, diphenhydramine hydrochloride) tablets is do not take more than directed (see overdose warning) adults and children 12 years and over take 2 caplets at bedtimedo not take more than 2 caplets of this product in 24 hours children under 12 years do not use. This formulation utilizes a tablet delivery system. Marketed by Cabinet Health P.b.c., this product is identified by NDC 82725-1024 and is authorized under FDA application M013.
Identification & Billing
- RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
- RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
- RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 82725 - Cabinet Health P.b.c.
- 82725-1024 - Valumeds Pain Relief Pm Pain Reliever And Nighttime Sleep Aid Acetaminophen, Extra Strength
- 82725-1024-1 - 375 TABLET in 1 BOTTLE
- 82725-1024 - Valumeds Pain Relief Pm Pain Reliever And Nighttime Sleep Aid Acetaminophen, Extra Strength
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 82725-1024-1 identifies a specific commercial package of 375 tablet in 1 bottle of Valumeds Pain Relief Pm Pain Reliever And Nighttime Sleep Aid Acetaminophen, Extra Strength, a human over the counter drug labeled by Cabinet Health P.b.c.. This tablet is formulated for oral use and contains acetaminophen; diphenhydramine hydrochloride 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 Cabinet Health P.b.c. on October 01, 2024. The current certification is valid through December 31, 2026.
How is this Cabinet Health P.b.c. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 82725102401. 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 Package segment to maintain the 5-4-2 structure.