NDC 83462-004 Beaueli 5% Minoxidil Hair Growth Oil

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:
83462-004
Proprietary Name:
Beaueli 5% Minoxidil Hair Growth Oil
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Labeler Code:
83462
Start Marketing Date: [9]
11-02-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
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Product Details

What is NDC 83462-004?

The NDC code 83462-004 is assigned by the FDA to the product Beaueli 5% Minoxidil Hair Growth Oil which is product labeled by Eubizrival Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83462-004-01 30 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 Beaueli 5% Minoxidil Hair Growth Oil?

. Apply 2-3 drops of serum directly to the scalp in the area to be treated. . Massage into the scalp with your fingers then wash hands thoroughly. - Using more hair regrowth serum or using the serum more often will not improve your results. . Continued use is necessary to increase and then maintain your hair regrowth. . Discontinuing use may result in hair loss.

Which are Beaueli 5% Minoxidil Hair Growth Oil UNII Codes?

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

Which are Beaueli 5% Minoxidil Hair Growth Oil 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:

What is the NDC to RxNorm Crosswalk for Beaueli 5% Minoxidil Hair Growth Oil?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".