70550-602 NDC - THICK HEAD EXTRA STRENGTH FOR MEN 5 MINOXIDIL TOPICAL (MINOXIDIL)

Drug Information

Product NDC: 70550-602
Proprietary Name: THICK HEAD Extra Strength for Men 5 Minoxidil Topical
Non Proprietary Name: MINOXIDIL
Active Ingredient(s): 5 g/100mL MINOXIDIL
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Pharmacy Class(es): Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	PROFECTUS BEAUTY, LLC
Product Type:	HUMAN OTC DRUG
FDA Application Number:	ANDA076239
Marketing Category:	ANDA
Start Marketing Date:	10/2/2023

Package Information

No.	Package Code	Package Description	Billing Unit
1	70550-602-01	1 BOTTLE, SPRAY in 1 BOX (70550-602-01) / 60 mL in 1 BOTTLE, SPRAY

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	70550-602	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PRODUCT TYPE NAME	HUMAN OTC DRUG	The translation of the dosage form Code submitted by the firm.
PROPRIETARY NAME	THICK HEAD Extra Strength for Men 5 Minoxidil Topical	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	MINOXIDIL	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
DOSAGE FORM NAME	SPRAY	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
ROUTE NAME	TOPICAL	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
START MARKETING DATE	10/2/2023
MARKETING CATEGORY NAME	ANDA	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
APPLICATION NUMBER	ANDA076239	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
LABELER NAME	PROFECTUS BEAUTY, LLC	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
SUBSTANCE NAME	MINOXIDIL	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
ACTIVE NUMERATOR STRENGTH	5
ACTIVE INGRED UNIT	g/100mL	The translation of the route code submitted by the firm, indicating route of administration.
PHARM CLASSES	Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]	This is the date that the labeler indicates was the start of its marketing of the drug product.

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This page was last updated on: 12/6/2025

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