Magictop Pain Relief Patch
NDC Package 72584-001-03

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Magictop Pain Relief Patch is adults (12 years and older)- Clean and dry the affected area.- Peel film off from patch and apply the herbal formula side onto skin.- Lasts for up to 24 hours; repeat as necessary and no less than 2 hours between applications.- For the best result, a 2-week course of treatment is recommended.- Children under 12 years: Consult your physician. Marketed by Zunyi Jici Bio-health Products Co Ltd, this product is identified by NDC 72584-001 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
72584-001-03
Package Description
3 BOX in 1 BOX / 3 PATCH in 1 BOX (72584-001-02) / 20 g in 1 PATCH (72584-001-01)
Product Code
72584-001
11-Digit Billing Format
72584000103
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Magictop Pain Relief Patch
Dosage Form
-
Usage Information
Adults (12 years and older)- Clean and dry the affected area.- Peel film off from patch and apply the herbal formula side onto skin.- Lasts for up to 24 hours; repeat as necessary and no less than 2 hours between applications.- For the best result, a 2-week course of treatment is recommended.- Children under 12 years: Consult your physician.

Regulatory & Marketing

Labeler Name
Zunyi Jici Bio-health Products Co Ltd
FDA Application #
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
12-28-2018
Listing Expiration
12-31-2020
Exclude Flag
I
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 72584-001-03 identifies a specific commercial package of 3 box in 1 box / 3 patch in 1 box (72584-001-02) / 20 g in 1 patch (72584-001-01) of Magictop Pain Relief Patch, labeled by Zunyi Jici Bio-health Products Co Ltd. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Zunyi Jici Bio-health Products Co Ltd on December 28, 2018. The current certification is valid through December 31, 2020.

How is this Zunyi Jici Bio-health Products Co Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72584000103. 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)
72584-001-03
11-Digit CMS (5-4-2)
72584-0001-03

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