Zhong Hua Jiu Patch
NDC Package 53614-001-02

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

Package Information

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

Zhong Hua Jiu Patch is aDULTS AND CHILDREN 12 YEARS OF AGE AND OLDER: REMOVE PATCH FROM THE PROTECTIVE LAYER, APPLY TO THE AFFECTED AREA, AND RUB THE AREA WITH YOUR HAND TO SECURE THE PATCH.PATCH WILL REMAIN EFFECTIVE FOR 12 HOURS AND WILL BE MROE EFFECTIVE WHEN USED 1 HOUR AFTER BATHING.DO NOT LEAVE THE PATCH ON THE SAME SPOT FOR MORE THAN 12 HOURS.DO NOT APPLY TO THE AREA WITH EXCESSIVE HAIR. Marketed by Wuhan Chinese Moxibustion Technology Development Co.; Ltd., this product is identified by NDC 53614-001 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
53614-001-02
Package Description
1000 mg in 1 PATCH
Product Code
11-Digit Billing Format
53614000102
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Zhong Hua Jiu Patch
Dosage Form
-
Usage Information
ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER: REMOVE PATCH FROM THE PROTECTIVE LAYER, APPLY TO THE AFFECTED AREA, AND RUB THE AREA WITH YOUR HAND TO SECURE THE PATCH.PATCH WILL REMAIN EFFECTIVE FOR 12 HOURS AND WILL BE MROE EFFECTIVE WHEN USED 1 HOUR AFTER BATHING.DO NOT LEAVE THE PATCH ON THE SAME SPOT FOR MORE THAN 12 HOURS.DO NOT APPLY TO THE AREA WITH EXCESSIVE HAIR. ADHESIVE PATCH MAY HURT SKIN UPON REMOVAL.CHILDREN UNDER 12 YEARS OF AGE: DO NOT USE OR CONSULT A DOCTOR.

Regulatory & Marketing

Labeler Name
Wuhan Chinese Moxibustion Technology Development 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
05-15-2003
Listing Expiration
12-31-2017
Exclude Flag
I
Sample Package
No

Hierarchy 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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 53614-001-02 identifies a specific commercial package of 1000 mg in 1 patch of Zhong Hua Jiu Patch, labeled by Wuhan Chinese Moxibustion Technology Development 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 Wuhan Chinese Moxibustion Technology Development Co.; Ltd. on May 15, 2003. The current certification is valid through December 31, 2017.

How is this Wuhan Chinese Moxibustion Technology Development Co.; Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53614000102. 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)
53614-001-02
11-Digit CMS (5-4-2)
53614-0001-02

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