Foot Rehab Pain Relief And Moisturizer
NDC Package 76347-120-01

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.

Foot Rehab Pain Relief And Moisturizer is stop use and ask a doctor if- condition worsens or symptoms persist for more than 7 days- Symptoms clear up and occur again within a few days.- excessive skin irritation occurs. Marketed by Mission Product Holdings, this product is identified by NDC 76347-120 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
76347-120-01
Package Description
85 g in 1 TUBE
Product Code
76347-120
11-Digit Billing Format
76347012001
RxNorm Crosswalk
  • RxCUI: 1358722 - Foot Rehab Pain & Moisture (menthol 10 % MG/ML / methyl salicylate 15 % ) Topical Cream
  • RxCUI: 1358722 - menthol 100 MG/ML / methyl salicylate 150 MG/ML Topical Cream [Foot Rehab Pain & Moisture]
  • RxCUI: 311498 - menthol 10 % / methyl salicylate 15 % Topical Cream
  • RxCUI: 311498 - menthol 100 MG/ML / methyl salicylate 150 MG/ML Topical Cream
  • RxCUI: 311498 - menthol 10 GM / methyl salicylate 15 GM per 100 GM Topical Cream

Clinical Specifications

Proprietary Name
Foot Rehab Pain Relief And Moisturizer Mission
Dosage Form
-
Usage Information
Stop use and ask a doctor if- condition worsens or symptoms persist for more than 7 days- Symptoms clear up and occur again within a few days.- excessive skin irritation occurs

Regulatory & Marketing

Labeler Name
Mission Product Holdings
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
11-05-2012
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 76347-120-01 identifies a specific commercial package of 85 g in 1 tube of Foot Rehab Pain Relief And Moisturizer Mission, labeled by Mission Product Holdings. 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 Mission Product Holdings on November 05, 2012. The current certification is valid through December 31, 2017.

How is this Mission Product Holdings product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76347012001. 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)
76347-120-01
11-Digit CMS (5-4-2)
76347-0120-01

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