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  5. NDC Package Code: 52261-4902-1 Asystem Radical Relief Gel Roll-on

NDC Package 52261-4902-1 Asystem Radical Relief Gel Roll-on

Menthol,Methyl Salicylate 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:
52261-4902-1
Package Description:
1 BOTTLE, WITH APPLICATOR in 1 CARTON / .075 kg in 1 BOTTLE, WITH APPLICATOR
Product Code:
52261-4902
Proprietary Name:
Asystem Radical Relief Gel Roll-on
Non-Proprietary Name:
Menthol, Methyl Salicylate
Substance Name:
Menthol; Methyl Salicylate
Usage Information:
Use only as directed.  Apply generously and massage to affected area as needed.  Do not use more than 3 to 4 times per day.  Children under 12 years of age ; ask a doctor before use.
11-Digit NDC Billing Format:
52261490201
NDC to RxNorm Crosswalk:
  • RxCUI: 282810 - menthol 10 % / methyl salicylate 15 % Topical Gel
  • RxCUI: 282810 - menthol 0.1 MG/MG / methyl salicylate 0.15 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Cosco International, Inc.
    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):
  • MENTHOL .1 kg/kg
  • METHYL SALICYLATE .15 kg/kg
    • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    07-03-2023
    Listing Expiration Date:
    12-31-2024
    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 52261-4902-1?

    The NDC Packaged Code 52261-4902-1 is assigned to a package of 1 bottle, with applicator in 1 carton / .075 kg in 1 bottle, with applicator of Asystem Radical Relief Gel Roll-on, a human over the counter drug labeled by Cosco International, Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 52261-4902 included in the NDC Directory?

    Yes, Asystem Radical Relief Gel Roll-on with product code 52261-4902 is active and included in the NDC Directory. The product was first marketed by Cosco International, Inc. on July 03, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 52261-4902-1?

    The 11-digit format is 52261490201. 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 5-4-1 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
    5-4-152261-4902-15-4-252261-4902-01