1. Home
  2. Labeler Index
  3. New Gpc, Inc.
  4. NDC Product Code: 65588-2230 Medisilke Night

NDC 65588-2230 Medisilke Night

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65588-2230?
  4. Medisilke Night 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:
65588-2230
Proprietary Name:
Medisilke Night
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
New Gpc, Inc.
Labeler Code:
65588
Product Label ID:
2e53471e-ad03-4d6b-9384-4af374bb5f74
Start Marketing Date: [9]
12-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 65588-2230?

The NDC code 65588-2230 is assigned by the FDA to the product Medisilke Night which is product labeled by New Gpc, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65588-2230-3 1 tube in 1 carton / 20 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 Medisilke Night?

Adults: apply a small amount as a thin layer on the affected area twice daily to affected area or use as directed by a physician. If no improvement is seen after 3 months of treatment, use of this product should 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.

Which are Medisilke Night UNII Codes?

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

Which are Medisilke Night 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".