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  4. NDC Product Code: 72650-080 Incellderm Dermatology First Package

NDC 72650-080 Incellderm Dermatology First Package

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72650-080?
  4. Incellderm Dermatology First Package 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:
72650-080
Proprietary Name:
Incellderm Dermatology First Package
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Riman Co., Ltd.
Labeler Code:
72650
Product Label ID:
540efa2b-d461-48b9-8d47-c12a1e8d75f5
Start Marketing Date: [9]
08-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 72650-080?

The NDC code 72650-080 is assigned by the FDA to the product Incellderm Dermatology First Package which is product labeled by Riman Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72650-080-01 1 kit in 1 box * 120 ml in 1 bottle, spray * 45 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 Incellderm Dermatology First Package?

Take an appropriate amount and spread it evenly over the skin.

Which are Incellderm Dermatology First Package UNII Codes?

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

Which are Incellderm Dermatology First Package 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".