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  4. NDC Product Code: 72044-105 Celderma Ninetalks Hydrogel Eye Patch Box

NDC 72044-105 Celderma Ninetalks Hydrogel Eye Patch Box

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72044-105?
  5. Celderma Ninetalks Hydrogel Eye Patch Box Uses
  6. Active Ingredients UNII Codes
  7. 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:
72044-105
Proprietary Name:
Celderma Ninetalks Hydrogel Eye Patch Box
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genic Co., Ltd
Labeler Code:
72044
Product Label ID:
69b056db-7594-3f49-e053-2991aa0adc36
Start Marketing Date: [9]
04-20-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Code Structure Chart

Product Details

What is NDC 72044-105?

The NDC code 72044-105 is assigned by the FDA to the product Celderma Ninetalks Hydrogel Eye Patch Box which is product labeled by Genic Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72044-105-03 4 pouch in 1 box / 1 patch in 1 pouch (72044-105-02) / 4.7 g in 1 patch (72044-105-01). 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 Celderma Ninetalks Hydrogel Eye Patch Box?

After cleansing, apply toner. Remove the film on the side of the eye patch, and apply it under the eye area for 20-40 minutes. Pat lightly to be absorbed the rest of residue. Recommended to use it 2-3 times a week.

Which are Celderma Ninetalks Hydrogel Eye Patch Box UNII Codes?

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

Which are Celderma Ninetalks Hydrogel Eye Patch Box 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".