Feminine Pain Relief Patch
NDC Package 71391-130-05

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

Package Information

Feminine Pain Relief (menthol, unspecified form) patches is for use by Adults and Children 12 years of age and olderApply to the affected area no more than 2 times a dayDry skin completely at application area, before applying the patchOpen pouch and remove patchPeel off protective film and apply sticky side to affected areaIf applied on hairy skin, remove gently using mild warm waterPatch once used, cannot be re-pasted or reusedDispose properly after use. This formulation utilizes a patch delivery system. Marketed by Unexo Life Sciences, Private Limited, this product is identified by NDC 71391-130 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
71391-130-05
Package Description
5 PATCH in 1 POUCH
Product Code
71391-130
11-Digit Billing Format
71391013005

Clinical Specifications

Proprietary Name
Feminine Pain Relief
Non-Proprietary Name
Menthol, Unspecified Form
Substance Name
Menthol, Unspecified Form
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, UNSPECIFIED FORM 200 mg/1
Usage Information
For use by Adults and Children 12 years of age and olderApply to the affected area no more than 2 times a dayDry skin completely at application area, before applying the patchOpen pouch and remove patchPeel off protective film and apply sticky side to affected areaIf applied on hairy skin, remove gently using mild warm waterPatch once used, cannot be re-pasted or reusedDispose properly after use

Regulatory & Marketing

Labeler Name
Unexo Life Sciences, Private Limited
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-19-2019
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 71391-130-05 identifies a specific commercial package of 5 patch in 1 pouch of Feminine Pain Relief, a human over the counter drug labeled by Unexo Life Sciences, Private Limited. This patch is formulated for topical use and contains menthol, unspecified form 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 Unexo Life Sciences, Private Limited on January 19, 2019. The current certification is valid through December 31, 2026.

How is this Unexo Life Sciences, Private Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71391013005. 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)
71391-130-05
11-Digit CMS (5-4-2)
71391-0130-05

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