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  4. NDC Product Code: 71483-0002 Teradia Diamond Intensive Hydrogel Eye

NDC 71483-0002 Teradia Diamond Intensive Hydrogel Eye

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71483-0002?
  4. Teradia Diamond Intensive Hydrogel Eye 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:
71483-0002
Proprietary Name:
Teradia Diamond Intensive Hydrogel Eye
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nanodia Lab Co Ltd
Labeler Code:
71483
Product Label ID:
60d3f3b0-b1de-629a-e053-2991aa0aec24
Start Marketing Date: [9]
12-20-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71483-0002?

The NDC code 71483-0002 is assigned by the FDA to the product Teradia Diamond Intensive Hydrogel Eye which is product labeled by Nanodia Lab Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71483-0002-1 90 g in 1 jar . 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 Teradia Diamond Intensive Hydrogel Eye?

After cleansing your face, apply toner with a cotton pad and sweep gently over face.Pick out a piece of eye patch on container.Attach the patch on the site you want like your around eyes, dark circle area and etc.Leave on for 10-15 minutes and remove the patch.Absorb the excess liquid by patting your around eyes

Which are Teradia Diamond Intensive Hydrogel Eye UNII Codes?

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

Which are Teradia Diamond Intensive Hydrogel Eye 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".