Flex24 Pain
NDC Package 73218-001-01

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.

Flex24 Pain is adults and children 2 years of age and older: Apply to the affected area not more than 3 times dailyChildren under 2 years old: consult a doctorTear and apply in a circle of 25 mm diameter to affected area and spread smoothly over the skin with fingersWash fingers that applied cream with water.  Do not rub eyes with fingers until washed with water. Marketed by Flex24, Inc., this product is identified by NDC 73218-001 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
73218-001-01
Package Description
3.8 g in 1 PACKET
Product Code
73218-001
11-Digit Billing Format
73218000101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Flex24 Pain
Dosage Form
-
Usage Information
Adults and children 2 years of age and older: Apply to the affected area not more than 3 times dailyChildren under 2 years old: consult a doctorTear and apply in a circle of 25 mm diameter to affected area and spread smoothly over the skin with fingersWash fingers that applied cream with water.  Do not rub eyes with fingers until washed with water

Regulatory & Marketing

Labeler Name
Flex24, Inc.
FDA Application #
part348
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
09-29-2019
Listing Expiration
12-31-2023
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 73218-001-01 identifies a specific commercial package of 3.8 g in 1 packet of Flex24 Pain, labeled by Flex24, Inc.. 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 Flex24, Inc. on September 29, 2019. The current certification is valid through December 31, 2023.

How is this Flex24, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73218000101. 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)
73218-001-01
11-Digit CMS (5-4-2)
73218-0001-01

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