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  4. NDC Product Code: 68634-051 Vividly Brilliant Perfecting

NDC 68634-051 Vividly Brilliant Perfecting

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68634-051?
  4. Vividly Brilliant Perfecting 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:
68634-051
Proprietary Name:
Vividly Brilliant Perfecting
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amcol Health & Beauty Solutions, Inc. Dba
Labeler Code:
68634
Product Label ID:
081cc08d-d9e9-4140-8c67-9b5fd998a5ff
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 68634-051?

The NDC code 68634-051 is assigned by the FDA to the product Vividly Brilliant Perfecting which is product labeled by Amcol Health & Beauty Solutions, Inc. Dba. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68634-051-01 1 bottle in 1 carton / 50 ml in 1 bottle. 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 Vividly Brilliant Perfecting?

Apply a single pump to face in the evening. If you have never used a retinol product before, begin by limiting use to twice a week, gradually increasing frequency to every other night, and then advancing to each evening or as tolerated. Mild redness, peeling and irritation is expected when using this product.

Which are Vividly Brilliant Perfecting UNII Codes?

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

Which are Vividly Brilliant Perfecting 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".