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

Camphor And Menthol Plaster Transdermal - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

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:
Proprietary Name:
Extra Strength Hua Tuo Pain Relieving
Non-Proprietary Name:
Camphor And Menthol
Substance Name:
Camphor (synthetic); Menthol
11-Digit NDC Billing Format:
69070030701
NDC to RxNorm Crosswalk:
  • RxCUI: 2118540 - camphor 3.1 % / menthol 2.6 % Medicated Patch
  • RxCUI: 2118540 - camphor 0.031 MG/MG / menthol 0.026 MG/MG Medicated Patch
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Zhejiang Dingtai Pharmaceutical Co., Ltd
    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(s):
  • Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
  • Sample Package:
    No
    FDA Application Number:
    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:
    04-09-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 69070-307-01?

    The NDC Packaged Code 69070-307-01 is assigned to a 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. The product's dosage form is plaster and is administered via transdermal form.

    Is NDC 69070-307 included in the NDC Directory?

    Yes, Extra Strength Hua Tuo Pain Relieving with product code 69070-307 is active and included in the NDC Directory. The product was first marketed by Zhejiang Dingtai Pharmaceutical Co., Ltd on April 09, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69070-307-01?

    The 11-digit format is 69070030701. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-269070-307-015-4-269070-0307-01