1. Home
  2. Labeler Index
  3. Gtg Wellness Co., Ltd.
  4. NDC Product Code: 71080-0027 Veclat Ou C.gnature 3 Power Radiant Face Mask

NDC 71080-0027 Veclat Ou C.gnature 3 Power Radiant Face Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71080-0027?
  4. Veclat Ou C.gnature 3 Power Radiant Face 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:
71080-0027
Proprietary Name:
Veclat Ou C.gnature 3 Power Radiant Face Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gtg Wellness Co., Ltd.
Labeler Code:
71080
Product Label ID:
308be053-f49b-4df2-914f-f6fed7f8601d
Start Marketing Date: [9]
11-01-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 71080-0027?

The NDC code 71080-0027 is assigned by the FDA to the product Veclat Ou C.gnature 3 Power Radiant Face Mask which is product labeled by Gtg Wellness Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71080-0027-2 4 pouch in 1 carton / 30 ml in 1 pouch (71080-0027-1). 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 Veclat Ou C.gnature 3 Power Radiant Face Mask?

■ Apply ampoule to the face and neck.■ Apply mask to skin and smooth to fit comfortably, leave on for 20 minutes, then peel off.■ Apply serum to the entire face and neck.

Which are Veclat Ou C.gnature 3 Power Radiant Face Mask UNII Codes?

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

Which are Veclat Ou C.gnature 3 Power Radiant Face 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:

* 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".