Pain Relief Pm Tablet
NDC Package 72090-032-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Pain Relief Pm (acetaminophen, diphenhydramine) tablets is ■ do not take more than directed (see overdose warning) adults and children 12 years and over■ take 2 caplets at bedtime ■ do not take more than 2 caplets in 24 hours unless directed by a doctor ■ children under 12 years do not use. This formulation utilizes a tablet delivery system. Marketed by Pioneer Life Sciences, Llc, this product is identified by NDC 72090-032 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
72090-032-01
Package Description
375 TABLET in 1 BOTTLE
Product Code
72090-032
11-Digit Billing Format
72090003201

Clinical Specifications

Proprietary Name
Pain Relief Pm
Non-Proprietary Name
Acetaminophen, Diphenhydramine
Substance Name
Acetaminophen; Diphenhydramine Hydrochloride
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
■ do not take more than directed (see overdose warning) adults and children 12 years and over■ take 2 caplets at bedtime ■ do not take more than 2 caplets in 24 hours unless directed by a doctor ■ children under 12 years do not use

Regulatory & Marketing

Labeler Name
Pioneer Life Sciences, Llc
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-29-2024
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72090-032-01 identifies a specific commercial package of 375 tablet in 1 bottle of Pain Relief Pm, a human over the counter drug labeled by Pioneer Life Sciences, Llc. 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 Pioneer Life Sciences, Llc on August 29, 2024. The current certification is valid through December 31, 2026.

How is this Pioneer Life Sciences, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72090003201. 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)
72090-032-01
11-Digit CMS (5-4-2)
72090-0032-01

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