Jimin Zhuifeng Gao
NDC Package 68048-822-01

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.

Jimin Zhuifeng Gao is adults and children 3 years of age and older, clean and dry the affected area, remove the paper backing from th plaste. Marketed by Guangdong Zhanjiang Jimin Pharmaceutical Co. Ltd, this product is identified by NDC 68048-822 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
68048-822-01
Package Description
10 PATCH in 1 BOX / 4 g in 1 PATCH
Product Code
68048-822
11-Digit Billing Format
68048082201
RxNorm Crosswalk
  • RxCUI: 1540676 - menthol 11 % / methyl salicylate 11 % Medicated Patch
  • RxCUI: 1540676 - menthol 0.11 MG/MG / methyl salicylate 0.11 MG/MG Medicated Patch

Clinical Specifications

Proprietary Name
Jimin Zhuifeng Gao
Dosage Form
-
Usage Information
Adults and children 3 years of age and older, clean and dry the affected area, remove the paper backing from th plaste. Apply the plaster to the affected area. Change plasters as needed, but do not apply more than 3 to 4 times daily.Children under 12 years of age: contact a doctor.

Regulatory & Marketing

Labeler Name
Guangdong Zhanjiang Jimin Pharmaceutical 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
07-01-2007
Listing Expiration
12-31-2017
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 68048-822-01 identifies a specific commercial package of 10 patch in 1 box / 4 g in 1 patch of Jimin Zhuifeng Gao, labeled by Guangdong Zhanjiang Jimin Pharmaceutical 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 Guangdong Zhanjiang Jimin Pharmaceutical Co. Ltd on July 01, 2007. The current certification is valid through December 31, 2017.

How is this Guangdong Zhanjiang Jimin Pharmaceutical Co. Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68048082201. 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)
68048-822-01
11-Digit CMS (5-4-2)
68048-0822-01

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