NDC 72044-106 Celderma Ninetalks Hydrogel Mask

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72044-106
Proprietary Name:
Celderma Ninetalks Hydrogel Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genic Co.,ltd
Labeler Code:
72044
Start Marketing Date: [9]
04-20-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 72044-106-03

Package Description: 4 POUCH in 1 BOX / 1 PATCH in 1 POUCH (72044-106-02) / 30 g in 1 PATCH (72044-106-01)

NDC Code 72044-106-04

Package Description: 30 g in 1 PATCH

Product Details

What is NDC 72044-106?

The NDC code 72044-106 is assigned by the FDA to the product Celderma Ninetalks Hydrogel Mask which is product labeled by Genic Co.,ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 72044-106-03 4 pouch in 1 box / 1 patch in 1 pouch (72044-106-02) / 30 g in 1 patch (72044-106-01), 72044-106-04 30 g in 1 patch . 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 Mask?

After cleansing, apply toner. Remove the film on the side of the mask, and apply the mask on face 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 Mask UNII Codes?

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

Which are Celderma Ninetalks Hydrogel Mask 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".