Pain Relief Gel-roll On Gel
NDC Package 73557-333-25

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

Package Information

Pain Relief Gel-roll On (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. This formulation utilizes a gel delivery system. Marketed by Shanghai Chuangshi Medical Technology (group) Co., Ltd., this product is identified by NDC 73557-333 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
73557-333-25
Package Description
74 mL in 1 BOTTLE
Product Code
73557-333
11-Digit Billing Format
73557033325
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Pain Relief Gel-roll On
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

Regulatory & Marketing

Labeler Name
Shanghai Chuangshi Medical Technology (group) Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-28-2022
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 73557-333-25 identifies a specific commercial package of 74 ml in 1 bottle of Pain Relief Gel-roll On, a human over the counter drug labeled by Shanghai Chuangshi Medical Technology (group) 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 Shanghai Chuangshi Medical Technology (group) Co., Ltd. on December 28, 2022. The current certification is valid through December 31, 2026.

How is this Shanghai Chuangshi Medical Technology (group) Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73557033325. 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)
73557-333-25
11-Digit CMS (5-4-2)
73557-0333-25

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