NDC 70889-910 Derma Eaude Glatok Cream

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:
70889-910
Proprietary Name:
Derma Eaude Glatok Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Oneskin Cosmetics Co., Ltd.
Labeler Code:
70889
Start Marketing Date: [9]
12-04-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 70889-910-10

Package Description: 1 CONTAINER in 1 BOX / 50 mL in 1 CONTAINER

Product Details

What is NDC 70889-910?

The NDC code 70889-910 is assigned by the FDA to the product Derma Eaude Glatok Cream which is product labeled by Oneskin Cosmetics Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70889-910-10 1 container in 1 box / 50 ml in 1 container. 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 Derma Eaude Glatok Cream?

Protects, restores and soothes the skinMoisturize and nourish the skinEnhances radiance and brightens skin

Which are Derma Eaude Glatok Cream UNII Codes?

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

Which are Derma Eaude Glatok Cream 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".