Dr.nuell Mugwort Shaking Pack
NDC Package 73430-0002-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Dr.nuell Mugwort Shaking Pack is 1. Marketed by Apharm Co., Ltd., this product is identified by NDC 73430-0002 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
73430-0002-1
Package Description
70 g in 1 PACKAGE
Product Code
11-Digit Billing Format
73430000201

Clinical Specifications

Proprietary Name
Dr.nuell Mugwort Shaking Pack
Dosage Form
-
Usage Information
1. put 1st and 2nd packs in the pouch and seal them and shake them for 10 seconds2. sweep the contents down and tear them along the bottom cut line3. apply mixture to the fact with a sqag-hola and gently remove it from the bottom to the top after 20~30 minutes4. remove the pack and apply skin product

Regulatory & Marketing

Labeler Name
Apharm Co., Ltd.
FDA Application #
part347
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
11-01-2019
Listing Expiration
12-31-2020
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 73430-0002-1 identifies a specific commercial package of 70 g in 1 package of Dr.nuell Mugwort Shaking Pack, labeled by Apharm 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 Apharm Co., Ltd. on November 01, 2019. The current certification is valid through December 31, 2020.

How is this Apharm Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73430000201. 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 (5-4-1)
73430-0002-1
11-Digit CMS (5-4-2)
73430-0002-01

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