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  4. NDC Product Code: 72650-020 Incellderm Dermatology Booster

NDC 72650-020 Incellderm Dermatology Booster

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72650-020?
  4. Incellderm Dermatology Booster 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:
72650-020
Proprietary Name:
Incellderm Dermatology Booster
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Riman Co., Ltd.
Labeler Code:
72650
Product Label ID:
d43ab97f-6b82-44cb-a1d6-975510b4de65
Start Marketing Date: [9]
03-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72650-020-01

Package Description: 120 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 72650-020?

The NDC code 72650-020 is assigned by the FDA to the product Incellderm Dermatology Booster 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 72650-020-01 120 ml in 1 bottle, spray . 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 Booster?

Directions:Take an appropriate amount and spread it evenly over the skin.Spray evenly around the area near the face and then do a daub.

Which are Incellderm Dermatology Booster UNII Codes?

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

Which are Incellderm Dermatology Booster 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".