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  4. NDC Product Code: 80592-201 Aqua De Folli Hair Booster Pro

NDC 80592-201 Aqua De Folli Hair Booster Pro

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80592-201?
  4. Aqua De Folli Hair Booster Pro 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:
80592-201
Proprietary Name:
Aqua De Folli Hair Booster Pro
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rokit Healthcare Inc.
Labeler Code:
80592
Product Label ID:
afe2470c-1e85-1e7e-e053-2995a90a2225
Start Marketing Date: [9]
09-24-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80592-201-01

Package Description: 3 mL in 1 BOTTLE

Product Details

What is NDC 80592-201?

The NDC code 80592-201 is assigned by the FDA to the product Aqua De Folli Hair Booster Pro which is product labeled by Rokit Healthcare Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80592-201-01 3 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 Aqua De Folli Hair Booster Pro?

- ​Apply 1 vial once a week directly onto the scalp in the hair loss area- Continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again

Which are Aqua De Folli Hair Booster Pro UNII Codes?

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

Which are Aqua De Folli Hair Booster Pro 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".