Pain Reliever / Fever Reducer
NDC Package 72090-002-01

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.

Pain Reliever / Fever Reducer is do not take more than directedthe smallest effective dose should be usedadults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persistif pain or fever does not respond to 1 tablet, 2 tablets may be useddo not exceed 6 tablets in 24 hours, unless directed by a doctorchildren under 12 years: ask a doctor. Marketed by Pioneer Life Sciences, Llc, this product is identified by NDC 72090-002 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
72090-002-01
Package Description
500 TABLET in 1 BOTTLE
Product Code
72090-002
11-Digit Billing Format
72090000201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Pain Reliever / Fever Reducer
Dosage Form
-
Usage Information
Do not take more than directedthe smallest effective dose should be usedadults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persistif pain or fever does not respond to 1 tablet, 2 tablets may be useddo not exceed 6 tablets in 24 hours, unless directed by a doctorchildren under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Pioneer Life Sciences, Llc
FDA Application #
part343
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
05-18-2021
Listing Expiration
12-31-2022
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 72090-002-01 identifies a specific commercial package of 500 tablet in 1 bottle of Pain Reliever / Fever Reducer, labeled by Pioneer Life Sciences, 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 Pioneer Life Sciences, Llc on May 18, 2021. The current certification is valid through December 31, 2022.

How is this Pioneer Life Sciences, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72090000201. 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)
72090-002-01
11-Digit CMS (5-4-2)
72090-0002-01

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