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  4. NDC Product Code: 77049-0011 The Fact-hfn Cooling Anti-hair Loss Tonicgel

NDC 77049-0011 The Fact-hfn Cooling Anti-hair Loss Tonicgel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77049-0011?
  4. The Fact-hfn Cooling Anti-hair Loss Tonicgel 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:
77049-0011
Proprietary Name:
The Fact-hfn Cooling Anti-hair Loss Tonicgel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Interkos Co.,ltd.
Labeler Code:
77049
Product Label ID:
d60f2989-5256-2873-e053-2995a90a775d
Start Marketing Date: [9]
01-21-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 77049-0011-1

Package Description: 150 mL in 1 BOTTLE

Product Details

What is NDC 77049-0011?

The NDC code 77049-0011 is assigned by the FDA to the product The Fact-hfn Cooling Anti-hair Loss Tonicgel which is product labeled by Interkos Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77049-0011-1 150 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 The Fact-hfn Cooling Anti-hair Loss Tonicgel?

After shampooing and before drying, apply an appropriate am ount to the scalp in a wet state using your fingers and massage so that it is fully absorbed. It ries commended to use it at least 3 times a week.

Which are The Fact-hfn Cooling Anti-hair Loss Tonicgel UNII Codes?

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

Which are The Fact-hfn Cooling Anti-hair Loss Tonicgel 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".