Thrulife Extra Strength Headache Relief
NDC Package 52605-014-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Thrulife Extra Strength Headache Relief is do not use more than directed ·drink a full glass of water with each dose ·adults and children 12 years and over: take 2 caplets every 6 hours: not more than 8 caplets in 24 hours ·children under  12 years of age: ask a doctor. Marketed by Polygen Pharmaceuticals Llc, this product is identified by NDC 52605-014 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
52605-014-01
Package Description
100 TABLET in 1 BOTTLE
Product Code
52605-014
11-Digit Billing Format
52605001401
RxNorm Crosswalk
  • RxCUI: 308297 - acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet
  • RxCUI: 308297 - APAP 250 MG / ASA 250 MG / caffeine 65 MG Oral Tablet

Clinical Specifications

Proprietary Name
Thrulife Extra Strength Headache Relief
Dosage Form
-
Usage Information
Do not use more than directed ·drink a full glass of water with each dose ·adults and children 12 years and over: take 2 caplets every 6 hours: not more than 8 caplets in 24 hours ·children under  12 years of age: ask a doctor.

Regulatory & Marketing

Labeler Name
Polygen Pharmaceuticals Llc
FDA Application #
part343
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-31-2013
Listing Expiration
12-31-2017
Exclude Flag
I
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 52605-014-01 identifies a specific commercial package of 100 tablet in 1 bottle of Thrulife Extra Strength Headache Relief, labeled by Polygen Pharmaceuticals Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Polygen Pharmaceuticals Llc on January 31, 2013. The current certification is valid through December 31, 2017.

How is this Polygen Pharmaceuticals Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52605001401. 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)
52605-014-01
11-Digit CMS (5-4-2)
52605-0014-01

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