Profoot Pain Relief Patches Kit
NDC Package 29784-600-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Profoot Pain Relief Patches (camphor, menthol, methyl salicylate) kits is uses For temporary relief of minor aches & pains of muscles & joints associated with: •arthritis •strains •bruises •sprains. This formulation utilizes a kit delivery system. Marketed by Rooftop Consumer Health, Inc., this product is identified by NDC 29784-600 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
29784-600-01
Package Description
1 KIT in 1 KIT * 4 PATCH in 1 KIT / .36 g in 1 PATCH (29784-121-36) * 2 PATCH in 1 KIT / 1.3 g in 1 PATCH (29784-122-36)
Product Code
29784-600
11-Digit Billing Format
29784060001
RxNorm Crosswalk
  • RxCUI: 853260 - camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated Patch
  • RxCUI: 853260 - camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated Patch

Clinical Specifications

Proprietary Name
Profoot Pain Relief Patches
Non-Proprietary Name
Camphor, Menthol, Methyl Salicylate
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Uses For temporary relief of minor aches & pains of muscles & joints associated with: •arthritis •strains •bruises •sprains

Regulatory & Marketing

Labeler Name
Rooftop Consumer Health, Inc.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-26-2018
End Marketing Date
05-31-2027
Exclude Flag
N
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 29784-600-01 identifies a specific commercial package of 1 kit in 1 kit * 4 patch in 1 kit / .36 g in 1 patch (29784-121-36) * 2 patch in 1 kit / 1.3 g in 1 patch (29784-122-36) of Profoot Pain Relief Patches, a human over the counter drug labeled by Rooftop Consumer Health, Inc.. This kit is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Rooftop Consumer Health, Inc. on September 26, 2018.

How is this Rooftop Consumer Health, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 29784060001. 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)
29784-600-01
11-Digit CMS (5-4-2)
29784-0600-01

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