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  4. NDC Product Code: 53010-3001 Jnh Ato-care Super Barried Ato-serum

NDC 53010-3001 Jnh Ato-care Super Barried Ato-serum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53010-3001?
  4. Jnh Ato-care Super Barried Ato-serum 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:
53010-3001
Proprietary Name:
Jnh Ato-care Super Barried Ato-serum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Daeduck Lab Co., Ltd
Labeler Code:
53010
Product Label ID:
dfcfea55-bc0e-4c9d-a519-96d4076546e5
Start Marketing Date: [9]
08-24-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 53010-3001?

The NDC code 53010-3001 is assigned by the FDA to the product Jnh Ato-care Super Barried Ato-serum which is product labeled by Daeduck Lab Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53010-3001-1 50 ml in 1 tube . 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 Jnh Ato-care Super Barried Ato-serum?

- Clean your skin first and apply the suitable amount of ATO serum, smoothly tap with fingers.- After taking a shower or washing your face, dry up water first then put the Serum where you feel dry or itchy.- If you ever feel dryness or sensitiveness from your skin, apply the Serum with controlling the amount.

Which are Jnh Ato-care Super Barried Ato-serum UNII Codes?

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

Which are Jnh Ato-care Super Barried Ato-serum 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".