The Goo Gel
NDC Package 82503-101-11

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

Package Information

The Goo (methyl salicylate, menthol, camphor) gel is adults and children over 12: Apply a thin layer and massage into painful area until thoroughly absorbed. This formulation utilizes a gel delivery system. Marketed by Apsm Performance, Llc, this product is identified by NDC 82503-101 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
82503-101-11
Package Description
100 mL in 1 BOTTLE
Product Code
82503-101
11-Digit Billing Format
82503010111
RxNorm Crosswalk
  • RxCUI: 1116730 - camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical Gel
  • RxCUI: 1116730 - camphor 0.04 MG/MG / menthol 0.1 MG/MG / methyl salicylate 0.3 MG/MG Topical Gel

Clinical Specifications

Proprietary Name
The Goo Medicated Pain Relief
Non-Proprietary Name
Methyl Salicylate, Menthol, Camphor
Substance Name
Camphor Oil; Menthol, Unspecified Form; Methyl Salicylate
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: Apply a thin layer and massage into painful area until thoroughly absorbed. Repeat as necessary, but no more than 4 times daily. After applying, wash hands with soap and water. Children under 12: Ask a doctor.

Regulatory & Marketing

Labeler Name
Apsm Performance, Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-30-2022
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 82503-101-11 identifies a specific commercial package of 100 ml in 1 bottle of The Goo Medicated Pain Relief, a human over the counter drug labeled by Apsm Performance, Llc. This gel is formulated for topical use and contains camphor oil; menthol, unspecified form; methyl salicylate 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 Apsm Performance, Llc on April 30, 2022. The current certification is valid through December 31, 2027.

How is this Apsm Performance, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82503010111. 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)
82503-101-11
11-Digit CMS (5-4-2)
82503-0101-11

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