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  4. NDC Product Code: 83299-016 5% Minoxidil Foam

NDC 83299-016 5% Minoxidil Foam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83299-016?
  4. 5% Minoxidil Foam 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 certification is expired.
NDC Product Code:
83299-016
Proprietary Name:
5% Minoxidil Foam
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Consilii Llc
Labeler Code:
83299
Product Label ID:
07430632-613f-01fa-e063-6294a90a25c8
Start Marketing Date: [9]
10-08-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
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Product Details

What is NDC 83299-016?

The NDC code 83299-016 is assigned by the FDA to the product 5% Minoxidil Foam which is product labeled by Consilii Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 83299-016-01 60 g in 1 bottle , 83299-016-02 60 g 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 5% Minoxidil Foam?

Apply half a capful 2 times a day directly to the scalp in the hair loss areaMassage into scalp with fingers, then wash wellUsing more than directed or more often will not improve results.Continued use is necessary to increase and then maintain your hair regrowth

Which are 5% Minoxidil Foam UNII Codes?

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

Which are 5% Minoxidil Foam 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".