Extra Strength Pain Reliever Capsule, Coated
NDC Package 73598-1372-1

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

Package Information

Extra Strength Pain Reliever (acetaminophen, aspirin, and caffeine) capsules is 2 tablets, with water every 6 hours while symptoms persist; not to exceed 8 tablets in 24 hours or as directed by a doctor. This formulation utilizes a capsule, coated delivery system. Marketed by Jhk Inc Dba American Safety & First Aid, this product is identified by NDC 73598-1372 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
73598-1372-1
Package Description
25 DOSE PACK in 1 BOX / 2 CAPSULE, COATED in 1 DOSE PACK
Product Code
73598-1372
11-Digit Billing Format
73598137201

Clinical Specifications

Proprietary Name
Extra Strength Pain Reliever
Non-Proprietary Name
Acetaminophen, Aspirin, And Caffeine
Substance Name
Acetaminophen; Aspirin; Caffeine
Dosage Form
Capsule, Coated - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container or "shell" made from a suitable form of gelatin; additionally, the capsule is covered in a designated coating.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
2 tablets, with water every 6 hours while symptoms persist; not to exceed 8 tablets in 24 hours or as directed by a doctor. Children under 12 years: consult a doctor.

Regulatory & Marketing

Labeler Name
Jhk Inc Dba American Safety & First Aid
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-02-2000
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 73598-1372-1 identifies a specific commercial package of 25 dose pack in 1 box / 2 capsule, coated in 1 dose pack of Extra Strength Pain Reliever, a human over the counter drug labeled by Jhk Inc Dba American Safety & First Aid. This capsule, coated is formulated for oral use and contains acetaminophen; aspirin; caffeine 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 Jhk Inc Dba American Safety & First Aid on February 02, 2000. The current certification is valid through December 31, 2026.

How is this Jhk Inc Dba American Safety & First Aid product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73598137201. 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 (5-4-1)
73598-1372-1
11-Digit CMS (5-4-2)
73598-1372-01

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