Shang Shi Zhi Tong Pain Relieving Plaster
NDC Package 51367-021-08

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.

Shang Shi Zhi Tong Pain Relieving Plaster is adults and children 12 years of age and older: apply one or two plasters to affected area once a day, remove after 8 hours.Children 2 to 12 years of age and adults with compromised health: use only under the guidance of a doctorChildren under 2 years of age: do not use. Marketed by International Nature Nutraceuticals, this product is identified by NDC 51367-021 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
51367-021-08
Package Description
8 PLASTER in 1 PACKAGE
Product Code
51367-021
11-Digit Billing Format
51367002108
RxNorm Crosswalk
  • RxCUI: 1547758 - camphor 3.5 % / menthol 2.3 % / methyl salicylate 14.6 % Medicated Patch
  • RxCUI: 1547758 - camphor 0.035 MG/MG / menthol 0.023 MG/MG / methyl salicylate 0.146 MG/MG Medicated Patch

Clinical Specifications

Proprietary Name
Shang Shi Zhi Tong Pain Relieving Plaster
Dosage Form
-
Usage Information
Adults and children 12 years of age and older: apply one or two plasters to affected area once a day, remove after 8 hours.Children 2 to 12 years of age and adults with compromised health: use only under the guidance of a doctorChildren under 2 years of age: do not use.

Regulatory & Marketing

Labeler Name
International Nature Nutraceuticals
FDA Application #
part348
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-16-1976
Listing Expiration
12-31-2025
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 51367-021-08 identifies a specific commercial package of 8 plaster in 1 package of Shang Shi Zhi Tong Pain Relieving Plaster, labeled by International Nature Nutraceuticals. 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 International Nature Nutraceuticals on August 16, 1976. The current certification is valid through December 31, 2025.

How is this International Nature Nutraceuticals product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51367002108. 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)
51367-021-08
11-Digit CMS (5-4-2)
51367-0021-08

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