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  4. NDC Product Code: 62742-4059 No Concealer Concealer

NDC 62742-4059 No Concealer Concealer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62742-4059?
  4. No Concealer Concealer 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:
62742-4059
Proprietary Name:
No Concealer Concealer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allure Labs, Inc
Labeler Code:
62742
Product Label ID:
911de0be-e169-4c47-a451-3a2601eba2ea
Start Marketing Date: [9]
12-09-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 62742-4059?

The NDC code 62742-4059 is assigned by the FDA to the product No Concealer Concealer which is product labeled by Allure Labs, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62742-4059-2 1 bottle, pump in 1 carton / 9 g in 1 bottle, pump (62742-4059-1). 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 No Concealer Concealer?

Uses:Helps prevent sunburn DIRECTIONS:Dr. Perricone recommends dispensing one pump, warmimg between ring fingers and patting gently along the lower eye contours, as well as upper eye lid and inner contours of eyes if desired. Any excess can also be applied on targeted areas of the face to cover imperfections.Apply generously and evenly 15 minutes before sun exposureUse a water resistant sunscreen if swimming or sweatingReapply atleast every two hoursNot for use on children

Which are No Concealer Concealer UNII Codes?

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

Which are No Concealer Concealer 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".