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  4. NDC Product Code: 50066-072 Teatrical Pro-aclarant Skin Lightening

NDC 50066-072 Teatrical Pro-aclarant Skin Lightening

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50066-072?
  5. Teatrical Pro-aclarant Skin Lightening Uses
  6. Active Ingredients UNII Codes
  7. 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:
50066-072
Proprietary Name:
Teatrical Pro-aclarant Skin Lightening
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genomma Lab Usa
Labeler Code:
50066
Product Label ID:
c20869a0-1b14-4df5-aeab-ce9c85513141
Start Marketing Date: [9]
04-22-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 50066-072?

The NDC code 50066-072 is assigned by the FDA to the product Teatrical Pro-aclarant Skin Lightening which is product labeled by Genomma Lab Usa. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50066-072-01 1 tube in 1 carton / 48 g 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 Teatrical Pro-aclarant Skin Lightening?

Adults: Apply a small amount as a thin layer on the affected area twice daily, or use as directed by a doctor. If no improvement is seen after 3 months of treatment, use of this product should be discontinued. Lightening effect of this product may not be noticeable when used on very dark skin.Children under 12 years of age: Do not use unless directed by a doctor.Exposure to the sun should be limited by using a sunscreen agent, sun blocking agent or protective clothing to cover bleached skin when using and after treatment is completed in order to prevent darkening from reoccurring.

Which are Teatrical Pro-aclarant Skin Lightening UNII Codes?

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

Which are Teatrical Pro-aclarant Skin Lightening 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".