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  5. NDC Package Code: 50231-521-11 Medistik Professional Dual Action

NDC Package 50231-521-11 Medistik Professional Dual Action

Methyl Salicylate,Menthol Spray 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:
50231-521-11
Package Description:
118 mL in 1 BOTTLE
Product Code:
50231-521
Proprietary Name:
Medistik Professional Dual Action
Non-Proprietary Name:
Methyl Salicylate, Menthol
Substance Name:
Menthol; Methyl Salicylate
Usage Information:
For use on adults and children over 12 years of age. For children (12 years old): Application should be supervised by an adult. Apply thinly and evenly to affected area up to 3 to 4 times per day. Rub and/or massage into skin until solution vanishes. A stinging or burning sensation will be experienced during the first few minutes as the formula begins working. For arthritis or muscle pain of the hands, retain for at least 10 minutes then wash hands. Consult your health care practitioner for use beyond 7 days
11-Digit NDC Billing Format:
50231052111
NDC to RxNorm Crosswalk:
  • RxCUI: 1738566 - menthol 10 % / methyl salicylate 12 % Topical Spray
  • RxCUI: 1738566 - menthol 100 MG/ML / methyl salicylate 120 MG/ML Topical Spray
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Natureteq Inc.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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 10 g/100mL
  • METHYL SALICYLATE 12 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-19-2016
    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 50231-521-11?

    The NDC Packaged Code 50231-521-11 is assigned to a package of 118 ml in 1 bottle of Medistik Professional Dual Action, a human over the counter drug labeled by Natureteq Inc.. The product's dosage form is spray and is administered via topical form.

    Is NDC 50231-521 included in the NDC Directory?

    Yes, Medistik Professional Dual Action with product code 50231-521 is active and included in the NDC Directory. The product was first marketed by Natureteq Inc. on February 19, 2016 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 50231-521-11?

    The 11-digit format is 50231052111. 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
    5-3-250231-521-115-4-250231-0521-11