Headache Relief Gel
NDC Package 59726-586-80

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

Package Information

Headache Relief (acetaminophen, aspirin, caffeine) gel is do not use more than directeddrink a full glass of water with each dose adults and children 12 years and over: take 2 geltabs every 6 hours; do not take more than 8 geltabs in 24 hours children under 12 years: do not use unless directed by a doctor. This formulation utilizes a gel delivery system. Marketed by P & L Development, Llc, this product is identified by NDC 59726-586 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
59726-586-80
Package Description
1 BOTTLE, PLASTIC in 1 BOTTLE / 80 GEL in 1 BOTTLE, PLASTIC
Product Code
59726-586
11-Digit Billing Format
59726058680

Clinical Specifications

Proprietary Name
Headache Relief Extra Strength
Non-Proprietary Name
Acetaminophen, Aspirin, Caffeine
Substance Name
Acetaminophen; Aspirin; Caffeine
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not use more than directeddrink a full glass of water with each dose adults and children 12 years and over: take 2 geltabs every 6 hours; do not take more than 8 geltabs in 24 hours children under 12 years: do not use unless directed by a doctor

Regulatory & Marketing

Labeler Name
P & L Development, Llc
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-20-2026
Listing Expiration
12-31-2027
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 59726-586-80 identifies a specific commercial package of 1 bottle, plastic in 1 bottle / 80 gel in 1 bottle, plastic of Headache Relief Extra Strength, a human over the counter drug labeled by P & L Development, Llc. This gel 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 P & L Development, Llc on June 20, 2026. The current certification is valid through December 31, 2027.

How is this P & L Development, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59726058680. 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)
59726-586-80
11-Digit CMS (5-4-2)
59726-0586-80

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