NDC 82372-005 5% Minoxidil Hair Growth Serum

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
82372-005
Proprietary Name:
5% Minoxidil Hair Growth Serum
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Code:
82372
Start Marketing Date: [9]
03-02-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Code Structure Chart

Product Details

What is NDC 82372-005?

The NDC code 82372-005 is assigned by the FDA to the product 5% Minoxidil Hair Growth Serum which is product labeled by Good Manager Holdings Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82372-005-02 60 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.

Which are 5% Minoxidil Hair Growth Serum UNII Codes?

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

Which are 5% Minoxidil Hair Growth Serum 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".