1. Home
  2. Labeler Index
  3. Acosmetic. Co.ltd
  4. NDC Product Code: 70961-0001 Deepair Micro Intensive Magic

NDC 70961-0001 Deepair Micro Intensive Magic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70961-0001?
  4. Deepair Micro Intensive Magic 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:
70961-0001
Proprietary Name:
Deepair Micro Intensive Magic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Acosmetic. Co.ltd
Labeler Code:
70961
Product Label ID:
3cc80bdc-214d-3d1b-e054-00144ff88e88
Start Marketing Date: [9]
08-01-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 70961-0001?

The NDC code 70961-0001 is assigned by the FDA to the product Deepair Micro Intensive Magic which is product labeled by Acosmetic. Co.ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70961-0001-1 2 pouch in 1 package / 2 patch in 1 pouch / 20 mg 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 Deepair Micro Intensive Magic?

Apply DEEPAIR MICRO INTENSIVE MAGIC CREAM before attaching the patches.Open the pouch.Remove the films.Attach the patches around the eye areas. Pat firm.Leave it for more than 30 minutes.

Which are Deepair Micro Intensive Magic UNII Codes?

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

Which are Deepair Micro Intensive Magic 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:

* Please review the disclaimer below.

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".