Good Remedies Extra Strength Pain Relief Pm Caplet Tablet
NDC Package 70692-741-03

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

Package Information

Good Remedies Extra Strength Pain Relief Pm Caplet (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 bedtime• do not take more than 2 caplets of this product in 24 hourschildren under 12 years  do not use. This formulation utilizes a tablet delivery system. Marketed by Strive Pharmaceuticals Inc., this product is identified by NDC 70692-741 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
70692-741-03
Package Description
1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
Product Code
11-Digit Billing Format
70692074103
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
Good Remedies Extra Strength Pain Relief Pm Caplet
Non-Proprietary Name
Acetaminophen, Diphenhydramine Hydrochloride
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.
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 of this product in 24 hourschildren under 12 years  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
03-17-2025
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 70692-741-03 identifies a specific commercial package of 1 bottle in 1 carton / 30 tablet in 1 bottle of Good Remedies Extra Strength Pain Relief Pm Caplet, a human over the counter drug labeled by Strive Pharmaceuticals Inc.. 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 Strive Pharmaceuticals Inc. on March 17, 2025. 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: 70692074103. 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)
70692-741-03
11-Digit CMS (5-4-2)
70692-0741-03

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