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  5. NDC Package Code: 82503-101-11 The Goo Medicated Pain Relief

NDC Package 82503-101-11 The Goo Medicated Pain Relief

Methyl Salicylate,Menthol,Camphor Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
82503-101-11
Package Description:
100 mL in 1 BOTTLE
Product Code:
82503-101
Proprietary Name:
The Goo Medicated Pain Relief
Non-Proprietary Name:
Methyl Salicylate, Menthol, Camphor
Substance Name:
Camphor Oil; Menthol, Unspecified Form; Methyl Salicylate
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.
11-Digit NDC Billing Format:
82503010111
NDC to 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
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Apsm Performance, Llc
    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(s):
  • 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):
  • CAMPHOR OIL 4 g/100mL
  • MENTHOL, UNSPECIFIED FORM 10 g/100mL
  • METHYL SALICYLATE 30 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-30-2022
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 82503-101-11?

    The NDC Packaged Code 82503-101-11 is assigned to a package of 100 ml in 1 bottle of The Goo Medicated Pain Relief, a human over the counter drug labeled by Apsm Performance, Llc. The product's dosage form is gel and is administered via topical form.

    Is NDC 82503-101 included in the NDC Directory?

    Yes, The Goo Medicated Pain Relief with product code 82503-101 is active and included in the NDC Directory. The product was first marketed by Apsm Performance, Llc on April 30, 2022 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 82503-101-11?

    The 11-digit format is 82503010111. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-282503-101-115-4-282503-0101-11