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  4. NDC Product Code: 73430-0002 Dr.nuell Mugwort Shaking Pack

NDC 73430-0002 Dr.nuell Mugwort Shaking Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73430-0002?
  4. Dr.nuell Mugwort Shaking Pack Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73430-0002
Proprietary Name:
Dr.nuell Mugwort Shaking Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apharm Co., Ltd.
Labeler Code:
73430
Product Label ID:
9669740b-c5ba-27e1-e053-2a95a90a7c31
Start Marketing Date: [9]
11-01-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73430-0002-1

Package Description: 70 g in 1 PACKAGE

Product Details

What is NDC 73430-0002?

The NDC code 73430-0002 is assigned by the FDA to the product Dr.nuell Mugwort Shaking Pack which is product labeled by Apharm Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73430-0002-1 70 g in 1 package . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Dr.nuell Mugwort Shaking Pack?

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

Which are Dr.nuell Mugwort Shaking Pack UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Dr.nuell Mugwort Shaking Pack Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".