Menthol Pain Relieving Gel
NDC Package 13709-357-01

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

Package Information

Menthol Pain Relieving Gel (pain relieving gel) gel is adults and Childern 2 years and olderClean skin thoroughly.Apply liberally to affected area not more than3-4 times daily.No Protective cover needed.May be used with ice packs.May be used with wet or dry bandages, but wrap loosely.Childern under 2 years of age. This formulation utilizes a gel delivery system. Marketed by Neilmed Pharmaceuticals Inc, this product is identified by NDC 13709-357 and is authorized under FDA application M014.

Identification & Billing

NDC Package Code
13709-357-01
Package Description
1 TUBE in 1 CARTON / 227 g in 1 TUBE
Product Code
13709-357
11-Digit Billing Format
13709035701
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Menthol Pain Relieving Gel
Non-Proprietary Name
Pain Relieving Gel
Substance Name
Menthol
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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 4.54 g/227g
Usage Information
Adults and Childern 2 years and olderClean skin thoroughly.Apply liberally to affected area not more than3-4 times daily.No Protective cover needed.May be used with ice packs.May be used with wet or dry bandages, but wrap loosely.Childern under 2 years of age.

Regulatory & Marketing

Labeler Name
Neilmed Pharmaceuticals Inc
Product Type
Human Otc Drug
FDA Application #
M014
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-07-2026
Listing Expiration
12-31-2027
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 13709-357-01 identifies a specific commercial package of 1 tube in 1 carton / 227 g in 1 tube of Menthol Pain Relieving Gel, a human over the counter drug labeled by Neilmed Pharmaceuticals Inc. This gel 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 Neilmed Pharmaceuticals Inc on May 07, 2026. The current certification is valid through December 31, 2027.

How is this Neilmed Pharmaceuticals Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 13709035701. 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)
13709-357-01
11-Digit CMS (5-4-2)
13709-0357-01

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