External Analgesic
NDC Package 73567-001-00

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.

External Analgesic is adults and children 12 years of age and older:Clean and dry affected area.Remove from backing film and apply.Remove from the skin after at most 8 hour's applicationApply to the affected area not more than 3 times daily.Children under 12 years of age: Consult a doctor. Marketed by Zhengzhou Daohe Medical Technology Co.,ltd, this product is identified by NDC 73567-001 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
73567-001-00
Package Description
1 PATCH in 1 POUCH / 8 mL in 1 PATCH
Product Code
73567-001
11-Digit Billing Format
73567000100
RxNorm Crosswalk
  • RxCUI: 1807136 - camphor 9.6 % / capsaicin 0.05 % / menthol 7.8 % Medicated Patch
  • RxCUI: 1807136 - camphor 0.096 MG/MG / capsaicin 0.0005 MG/MG / menthol 0.078 MG/MG Medicated Patch

Clinical Specifications

Proprietary Name
External Analgesic
Dosage Form
-
Usage Information
Adults and children 12 years of age and older:Clean and dry affected area.Remove from backing film and apply.Remove from the skin after at most 8 hour's applicationApply to the affected area not more than 3 times daily.Children under 12 years of age: Consult a doctor.

Regulatory & Marketing

Labeler Name
Zhengzhou Daohe Medical Technology Co.,ltd
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-2020
Listing Expiration
12-31-2024
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 73567-001-00 identifies a specific commercial package of 1 patch in 1 pouch / 8 ml in 1 patch of External Analgesic, labeled by Zhengzhou Daohe Medical Technology 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 Zhengzhou Daohe Medical Technology Co.,ltd on April 01, 2020. The current certification is valid through December 31, 2024.

How is this Zhengzhou Daohe Medical Technology Co.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73567000100. 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)
73567-001-00
11-Digit CMS (5-4-2)
73567-0001-00

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