NDC 73430-0002 Dr.nuell Mugwort Shaking Pack

Product Information

Product Code73430-0002
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Dr.nuell Mugwort Shaking Pack
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Apharm Co., Ltd.
Labeler Code73430
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 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.
Exclude Flag 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".
NDC Code Structure

Usage Information

Product Packages

NDC 73430-0002-1

Package Description: 70 g in 1 PACKAGE

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

Product Details

Dr.nuell Mugwort Shaking Pack is product labeled by Apharm Co., Ltd.. The product's dosage form is and is administered via form.

What are Dr.nuell Mugwort Shaking Pack Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)

Inactive Ingredient(s)

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.

  • ALLANTOIN (UNII: 344S277G0Z)

* Please review the disclaimer below.

Dr.nuell Mugwort Shaking Pack Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents

Otc - Active Ingredient


Otc - Purpose

dual functionality for brightening and wrinkle improvement certified

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

1. put 1st and 2nd packs in the pouch and seal them and shake them for 10 seconds

2. sweep the contents down and tear them along the bottom cut line

3. apply mixture to the fact with a sqag-hola and gently remove it from the bottom to the top after 20~30 minutes

4. remove the pack and apply skin product


1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists
2) Do not use for wounded areas
3) Precautions for storage and handling
keep out of reach of children, store away from direct sunlight
4) avoid the eye area

Inactive Ingredient

water, butylene glycol, 1,2-hexanediol, citric acid, etc

Dosage & Administration

For external use only

Package Label.Principal Display Panel

* Please review the disclaimer below.