NDC 83299-018 5% Minoxidil 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:
83299-018
Proprietary Name:
5% Minoxidil Serum
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Labeler Code:
83299
Start Marketing Date: [9]
10-31-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
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Product Details

What is NDC 83299-018?

The NDC code 83299-018 is assigned by the FDA to the product 5% Minoxidil Serum which is product labeled by Consilii Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83299-018-01 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.

What are the uses for 5% Minoxidil Serum?

Sterilize the roller with alcohol before useClean the skin area and dry itApply roller gently on your skin, roll diagnoally, horizontally & vertically 4-5 times on target areasApply 2-3 drops of serum directly to the scalp in the area to be treatedMassage into the scalp with your finger then wash hand thoroughlyAlways perform the test on a small area of the skin to make sure there is no allergic reactionInitial shedding may occur as the new hairs push out older strands.

Which are 5% Minoxidil Serum UNII Codes?

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

Which are 5% Minoxidil 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:

What is the NDC to RxNorm Crosswalk for 5% Minoxidil Serum?

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".