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  4. NDC Product Code: 72160-0001 Premiu Serum Mask

NDC 72160-0001 Premiu Serum Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72160-0001?
  4. Premiu Serum Mask 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:
72160-0001
Proprietary Name:
Premiu Serum Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Inano Co., Ltd.
Labeler Code:
72160
Product Label ID:
672c83fb-666f-5ba0-e053-2991aa0ab239
Start Marketing Date: [9]
03-12-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72160-0001-1

Package Description: 25 g in 1 POUCH

Product Details

What is NDC 72160-0001?

The NDC code 72160-0001 is assigned by the FDA to the product Premiu Serum Mask which is product labeled by Inano Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72160-0001-1 25 g 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 Premiu Serum Mask?

1. after washing, remove moisture entirely to arrange skin texture2. apply the wine gold serum (step 1) onto the face equaly and rub the serum softly like massae to absorb perfectly3. unfolding the mask (step 2), position the mask on the fact according to position of eyes and mouth4. remove the mask sheet after 15~30 minutes, after that softly pat any remaining essence into skin like massage

Which are Premiu Serum Mask UNII Codes?

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

Which are Premiu Serum 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".