Pain Reliever
NDC Package 49348-709-59

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 discontinued by the firm.

Pain Reliever is a medication used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever. Marketed by Mckesson (sunmark), this product is identified by NDC 49348-709 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
49348-709-59
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Product Code
49348-709
11-Digit Billing Format
49348070959

Clinical Specifications

Proprietary Name
Pain Reliever Extra Strength
Dosage Form
-
Usage Information
This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.

Regulatory & Marketing

Labeler Name
Mckesson (sunmark)
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
07-09-2010
End Marketing Date
03-31-2019
Listing Expiration
03-31-2019
Exclude Flag
D
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 49348-709-59 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 40 capsule, liquid filled in 1 bottle, plastic of Pain Reliever Extra Strength, labeled by Mckesson (sunmark). 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 Mckesson (sunmark) on July 09, 2010. The current certification is valid through March 31, 2019.

What are the primary indications for this medication?

This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.

How is this Mckesson (sunmark) product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49348070959. 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)
49348-709-59
11-Digit CMS (5-4-2)
49348-0709-59

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