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  4. NDC Product Code: 62742-4044 Clear Cell Medicated Acne Masque

NDC 62742-4044 Clear Cell Medicated Acne Masque

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62742-4044?
  4. Clear Cell Medicated Acne Masque Uses
  5. Active 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:
62742-4044
Proprietary Name:
Clear Cell Medicated Acne Masque
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allure Labs, Inc.
Labeler Code:
62742
Product Label ID:
720ee542-01a9-4aa5-b95c-571e947fbac7
Start Marketing Date: [9]
01-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62742-4044-1

Package Description: 56.7 mL in 1 TUBE

Product Details

What is NDC 62742-4044?

The NDC code 62742-4044 is assigned by the FDA to the product Clear Cell Medicated Acne Masque 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 62742-4044-1 56.7 ml in 1 tube . 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 Clear Cell Medicated Acne Masque?

INDICATIONS AND USAGE SECTION:An aha/bha blended acne masque designed to immediately draw out impurities and excess oil. Anti-oxidant blends of nutrients soothe irritated and red acne lesions. This amazing masque leaves skin fresh and oil-free.Paraben-freeDIRECTIONS:Apply to cleansed skin for 5-15 minutes, remove with tepid water, followed by a cold water splash. May be used as a spot treatment for active lesions.INDICATIONS:Acne and acne-prone skin

Which are Clear Cell Medicated Acne Masque UNII Codes?

The UNII codes for the active 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".