Relief Patch
NDC Package 72587-003-01

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

Package Information

Relief (menthol) patches is adults over 18 years:use one patchcarefully remove the backing film and apply to the affected area no more than 3 to 4 times dailyeach patch can be worn up to 12 hourschildren under 18 years of age: consult a doctor. This formulation utilizes a patch delivery system. Marketed by La Mend, Inc., this product is identified by NDC 72587-003 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
72587-003-01
Package Description
4 PATCH in 1 POUCH / 1 g in 1 PATCH
Product Code
72587-003
11-Digit Billing Format
72587000301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Relief
Non-Proprietary Name
Menthol
Substance Name
Menthol
Dosage Form
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
MENTHOL 5 g/100g
Usage Information
Adults over 18 years:use one patchcarefully remove the backing film and apply to the affected area no more than 3 to 4 times dailyeach patch can be worn up to 12 hourschildren under 18 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
La Mend, Inc.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-01-2024
Listing Expiration
12-31-2026
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 72587-003-01 identifies a specific commercial package of 4 patch in 1 pouch / 1 g in 1 patch of Relief, a human over the counter drug labeled by La Mend, Inc.. This patch is formulated for topical use and contains menthol 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 La Mend, Inc. on August 01, 2024. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72587000301. 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)
72587-003-01
11-Digit CMS (5-4-2)
72587-0003-01

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