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  4. NDC Product Code: 82934-301 Dr. Zonskin Nunssup Jara

NDC 82934-301 Dr. Zonskin Nunssup Jara

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82934-301?
  4. Dr. Zonskin Nunssup Jara 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:
82934-301
Proprietary Name:
Dr. Zonskin Nunssup Jara
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
J 1010 Co., Ltd.
Labeler Code:
82934
Product Label ID:
e70c0318-aa6d-17d1-e053-2995a90a8669
Start Marketing Date: [9]
08-25-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 82934-301-01

Package Description: 7 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 82934-301?

The NDC code 82934-301 is assigned by the FDA to the product Dr. Zonskin Nunssup Jara which is product labeled by J 1010 Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82934-301-01 7 ml in 1 bottle, with applicator . 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. Zonskin Nunssup Jara?

Use a brush to get an appropriate amount of serum and apply it to the eyelash from the root to the tip.

Which are Dr. Zonskin Nunssup Jara UNII Codes?

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

Which are Dr. Zonskin Nunssup Jara 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".