NDC 70905-0018 Dr.althea Premium Intensive Essence 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:
70905-0018
Proprietary Name:
Dr.althea Premium Intensive Essence Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dr. Althea
Labeler Code:
70905
Start Marketing Date: [9]
08-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70905-0018-1

Package Description: 14 POUCH in 1 PACKAGE / 2 mL in 1 POUCH

Product Details

What is NDC 70905-0018?

The NDC code 70905-0018 is assigned by the FDA to the product Dr.althea Premium Intensive Essence Mask which is product labeled by Dr. Althea. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70905-0018-1 14 pouch in 1 package / 2 ml in 1 pouch. 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 Dr.althea Premium Intensive Essence Mask?

[How To Use] After prepping cleansed face with a toner, apply an appropriate amount of Essence Mask on the face and gently massage it until it is fully absorbed into the skin. Considering the skin restoring cycle and for full benefits, use 3~4 pouches a week for four consecutive weeks.

Which are Dr.althea Premium Intensive Essence Mask UNII Codes?

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

Which are Dr.althea Premium Intensive Essence 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".