Menthol Pain Relief Gel-tube Gel
NDC Package 83602-323-30

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

Package Information

Menthol Pain Relief Gel-tube (menthol) gel is adults and children 12 years of age and older:• Rub a thin film over affected areas not more than 4 times daily;• Message not necessaryChildren under 12 years of age: Consult physician.Wash hands after use with cool water. This formulation utilizes a gel delivery system. Marketed by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd., this product is identified by NDC 83602-323 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
83602-323-30
Package Description
89 mL in 1 TUBE
Product Code
83602-323
11-Digit Billing Format
83602032330
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Menthol Pain Relief Gel-tube
Non-Proprietary Name
Menthol
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 .04 g/mL
Usage Information
Adults and children 12 years of age and older:• Rub a thin film over affected areas not more than 4 times daily;• Message not necessaryChildren under 12 years of age: Consult physician.Wash hands after use with cool water.

Regulatory & Marketing

Labeler Name
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-06-2023
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 83602-323-30 identifies a specific commercial package of 89 ml in 1 tube of Menthol Pain Relief Gel-tube, a human over the counter drug labeled by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.. 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 Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. on December 06, 2023. The current certification is valid through December 31, 2026.

How is this Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83602032330. 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)
83602-323-30
11-Digit CMS (5-4-2)
83602-0323-30

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