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  5. NDC Package Code: 59088-954-05 Myorx Low Dose Pain Relieving

NDC Package 59088-954-05 Myorx Low Dose Pain Relieving

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
59088-954-05
Package Description:
59 mL in 1 JAR
Product Code:
59088-954
Proprietary Name:
Myorx Low Dose Pain Relieving
Usage Information:
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.Children under 2 years of age: consult a doctor.
11-Digit NDC Billing Format:
59088095405
NDC to RxNorm Crosswalk:
  • RxCUI: 1114454 - menthol 0.5 % Topical Cream
  • RxCUI: 1114454 - menthol 5 MG/ML Topical Cream
  • RxCUI: 1114456 - Myorx 0.5 % Topical Cream
  • RxCUI: 1114456 - menthol 5 MG/ML Topical Cream [Myorx]
  • RxCUI: 1114456 - Myorx 5 MG/ML Topical Cream
    • Labeler Name:
    Puretek Corporation
    Sample Package:
    No
    Start Marketing Date:
    07-01-2011
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 59088-954-05?

    The NDC Packaged Code 59088-954-05 is assigned to a package of 59 ml in 1 jar of Myorx Low Dose Pain Relieving, labeled by Puretek Corporation. The product's dosage form is and is administered via form.

    Is NDC 59088-954 included in the NDC Directory?

    No, Myorx Low Dose Pain Relieving with product code 59088-954 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Puretek Corporation on July 01, 2011 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 59088-954-05?

    The 11-digit format is 59088095405. 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
    5-3-259088-954-055-4-259088-0954-05