Cooling Pain Relief Gel
NDC Package 49283-581-20

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

Package Information

Cooling Pain Relief (menthol, camphor) gel is adults and children over 12 yearsApply a small amount on the affected area.Massage in a circular motion until absorbed, let set for a few seconds.Repeat as needed, but no more than 3 to 4 times per day.Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).Wash hands with soap and water after use.Children under 12 years of age consult a doctor. This formulation utilizes a gel delivery system. Marketed by Chemco Corporation, this product is identified by NDC 49283-581 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
49283-581-20
Package Description
59 mL in 1 TUBE
Product Code
49283-581
11-Digit Billing Format
49283058120

Clinical Specifications

Proprietary Name
Cooling Pain Relief
Non-Proprietary Name
Menthol, Camphor
Substance Name
Camphor (synthetic); 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)
Usage Information
Adults and children over 12 yearsApply a small amount on the affected area.Massage in a circular motion until absorbed, let set for a few seconds.Repeat as needed, but no more than 3 to 4 times per day.Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).Wash hands with soap and water after use.Children under 12 years of age consult a doctor.

Regulatory & Marketing

Labeler Name
Chemco Corporation
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-29-2026
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 49283-581-20 identifies a specific commercial package of 59 ml in 1 tube of Cooling Pain Relief, a human over the counter drug labeled by Chemco Corporation. This gel is formulated for topical use and contains camphor (synthetic); 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 Chemco Corporation on January 29, 2026. The current certification is valid through December 31, 2027.

How is this Chemco Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49283058120. 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)
49283-581-20
11-Digit CMS (5-4-2)
49283-0581-20

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