Extra Strength Hua Tuo Pain Relieving Plaster
NDC Package 69070-307-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Extra Strength Hua Tuo Pain Relieving (camphor and menthol) plasters is a human otc drug administered via transdermal route. This formulation utilizes a plaster delivery system. Marketed by Zhejiang Dingtai Pharmaceutical Co., Ltd, this product is identified by NDC 69070-307 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
69070-307-01
Package Description
1 POUCH in 1 BOX / 5 PATCH in 1 POUCH / 1 g in 1 PATCH
Product Code
69070-307
11-Digit Billing Format
69070030701
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Extra Strength Hua Tuo Pain Relieving
Non-Proprietary Name
Camphor And Menthol
Substance Name
Camphor (synthetic); Menthol
Dosage Form
Plaster - Substance intended for external application made of such materials and of such consistency as to adhere to the skin and attach to a dressing; plasters are intended to afford protection and support and/or to furnish an occlusion and macerating action and to bring medication into close contact with the skin.
Administration Route
Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
Active Ingredient(s)

Regulatory & Marketing

Labeler Name
Zhejiang Dingtai Pharmaceutical Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-09-2019
Listing Expiration
12-31-2026
Exclude Flag
N
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 69070-307-01 identifies a specific commercial package of 1 pouch in 1 box / 5 patch in 1 pouch / 1 g in 1 patch of Extra Strength Hua Tuo Pain Relieving, a human over the counter drug labeled by Zhejiang Dingtai Pharmaceutical Co., Ltd. This plaster is formulated for transdermal use and contains camphor (synthetic); menthol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Zhejiang Dingtai Pharmaceutical Co., Ltd on April 09, 2019. The current certification is valid through December 31, 2026.

How is this Zhejiang Dingtai Pharmaceutical Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69070030701. 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)
69070-307-01
11-Digit CMS (5-4-2)
69070-0307-01

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