Right Remedies Extra Strength Pm Pain Relief Tablet, Film Coated
NDC Package 70692-149-31

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Right Remedies Extra Strength Pm Pain Relief (acetaminophen, diphenhydramine hydrochloride) tablets is • do not take more than directed (see overdose warning) • do not take more than 2 caplets in 24 hours adults & children 12 years of age and over • take 2 caplets at bedtime • do not take more than 2 caplets of this product in 24 hours children under 12 years of age do not use. This formulation utilizes a tablet, film coated delivery system. Marketed by Strive Pharmaceuticals Inc., this product is identified by NDC 70692-149 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
70692-149-31
Package Description
300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
70692014931
RxNorm Crosswalk
  • 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

Proprietary Name
Right Remedies Extra Strength Pm Pain Relief
Non-Proprietary Name
Acetaminophen, Diphenhydramine Hydrochloride
Substance Name
Acetaminophen; Diphenhydramine Hydrochloride
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
• do not take more than directed (see overdose warning) • do not take more than 2 caplets in 24 hours adults & children 12 years of age and over • take 2 caplets at bedtime • do not take more than 2 caplets of this product in 24 hours children under 12 years of age do not use

Regulatory & Marketing

Labeler Name
Strive Pharmaceuticals Inc.
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-13-2023
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (70692-149). Click a package code to view its specific billing and regulatory data.

1 BOTTLE, PLASTIC in 1 CARTON / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 CARTON / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

* 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 70692-149-31 identifies a specific commercial package of 300 tablet, film coated in 1 bottle, plastic of Right Remedies Extra Strength Pm Pain Relief, a human over the counter drug labeled by Strive Pharmaceuticals Inc.. This tablet, film coated 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 Strive Pharmaceuticals Inc. on November 13, 2023. The current certification is valid through December 31, 2026.

How is this Strive Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70692014931. 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)
70692-149-31
11-Digit CMS (5-4-2)
70692-0149-31

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