Heibaitong Pain Relieving Patch
NDC Package 72328-001-01

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.

Heibaitong Pain Relieving Patch is adults and children 12 years of age and older: This product can be applied up to 168 hours of repeated uses. Marketed by Harbin Kangyou Pharmaceutical Limited Company, this product is identified by NDC 72328-001 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
72328-001-01
Package Description
1 PATCH in 1 POUCH / 13 g in 1 PATCH
Product Code
72328-001
11-Digit Billing Format
72328000101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Heibaitong Pain Relieving Patch
Dosage Form
-
Usage Information
Adults and children 12 years of age and older: This product can be applied up to 168 hours of repeated uses. Remove the package from package. Heat up the patch until it easily gets separated and it becomes soft and glossy. Apply one or two patches to affected area once a day. Remove after every 6-12 hours depending on symptoms. Children 2 to 12 years of age and adults with compromised health: Use only under the guidance of a doctor. Children under 2 years of age: Do not use, consult a doctor. Refer to the above warnings: use otherwise than as directed may be dangerous.

Regulatory & Marketing

Labeler Name
Harbin Kangyou Pharmaceutical Limited Company
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
07-23-2018
Listing Expiration
12-31-2019
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 72328-001-01 identifies a specific commercial package of 1 patch in 1 pouch / 13 g in 1 patch of Heibaitong Pain Relieving Patch, labeled by Harbin Kangyou Pharmaceutical Limited Company. 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 Harbin Kangyou Pharmaceutical Limited Company on July 23, 2018. The current certification is valid through December 31, 2019.

How is this Harbin Kangyou Pharmaceutical Limited Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72328000101. 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)
72328-001-01
11-Digit CMS (5-4-2)
72328-0001-01

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