Medrox
NDC Package 50436-9991-1

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.

Medrox is adults and children 12 years and over apply to affected area: change patch 1 to 2 times dailyChildren under 12 years, consult physician before useHow to apply:Clean and dry affected areaCut open pouch and remove patchRemove protective film and apply directly to area of painApply to affected area not more than 3 times dailyWash hands with soap after applying patchReseal pouch containing unused patches. Marketed by Unit Dose Services, this product is identified by NDC 50436-9991 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
50436-9991-1
Package Description
5 g in 1 BOX
Product Code
50436-9991
11-Digit Billing Format
50436999101
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA
RxNorm Crosswalk
  • RxCUI: 1300889 - capsaicin 0.0375 % / menthol 5 % Medicated Patch
  • RxCUI: 1300889 - capsaicin 0.000375 MG/MG / menthol 0.05 MG/MG Medicated Patch

Clinical Specifications

Proprietary Name
Medrox
Dosage Form
-
Usage Information
Adults and children 12 years and over apply to affected area: change patch 1 to 2 times dailyChildren under 12 years, consult physician before useHow to apply:Clean and dry affected areaCut open pouch and remove patchRemove protective film and apply directly to area of painApply to affected area not more than 3 times dailyWash hands with soap after applying patchReseal pouch containing unused patches

Regulatory & Marketing

Labeler Name
Unit Dose Services
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
06-13-2012
Listing Expiration
12-31-2019
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 50436-9991-1 identifies a specific commercial package of 5 g in 1 box of Medrox, labeled by Unit Dose Services. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. 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 Unit Dose Services on June 13, 2012. The current certification is valid through December 31, 2019.

How is this Unit Dose Services product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50436999101. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. 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 (5-4-1)
50436-9991-1
11-Digit CMS (5-4-2)
50436-9991-01

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