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  4. NDC Product Code: 71224-0003 Perfect V Lifting Premium Black Mask

NDC 71224-0003 Perfect V Lifting Premium Black Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71224-0003?
  4. Perfect V Lifting Premium Black 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:
71224-0003
Proprietary Name:
Perfect V Lifting Premium Black Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avajar Co Ltd
Labeler Code:
71224
Product Label ID:
62764270-0f8f-269e-e053-2991aa0ad2c6
Start Marketing Date: [9]
01-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 71224-0003?

The NDC code 71224-0003 is assigned by the FDA to the product Perfect V Lifting Premium Black Mask which is product labeled by Avajar Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71224-0003-1 5 patch in 1 package / 11 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 Perfect V Lifting Premium Black Mask?

1. Open the pouch and remove the protective film.2. After stretching the mask, put your chin on the middle of the mask.3. After matching your chin to the middle of the mask, hook onto the ears.4. After 1-2 hours of use, remove the mask and lightly massge both cheeks.

Which are Perfect V Lifting Premium Black Mask UNII Codes?

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

Which are Perfect V Lifting Premium Black 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".