FINASTERIDE 0.1% / MINOXIDIL 5%

Manufacturer: Sincerus Florida, LLC
Effective date: 2019-05-08
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 20:28:38

Label at a glance#

ProductFINASTERIDE 0.1% / MINOXIDIL 5%

Active ingredientMINOXIDIL, FINASTERIDE

Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

Sincerus Florida, LLC

ADVERSE REACTIONS SECTION

Active, inactive

COMPONENTS

;klm

NDC 72934-4074-8. FINASTERIDE USP 0.1% / MINOXIDIL USP 5%. Solution 60 gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
FINASTERIDE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813
MINOXIDIL Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
928d249c-35c3-4d88-a9ef-cf2f2e31b96f	Product name	1	20220706
d00474ae-23eb-a8eb-bf56-520e590cc6db	Product name	2	20170406
0f90664c-9d0e-f046-dc6a-73563cd8347e	Product name	2	20170405

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72934-4074-8	2021-01-29	C162847	48780-1	ba0f9c33-4fd0-a910-e053-dadaa90a0b85	FINASTERIDE 0.1% / MINOXIDIL 5%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72934-4074-8	FINASTERIDE 0.1% / MINOXIDIL 5%	60 g in 1 BOTTLE, GLASS	SOLUTION	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72934-4074	FINASTERIDE 0.1% / MINOXIDIL 5% SOLUTION [SINCERUS FLORIDA, LLC]	1	Legacy NDC, 1 package rows	20190509_8861f646-2de0-e95c-e053-2a95a90a2041.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

FINASTERIDE 0.1% / MINOXIDIL 5%
MINOXIDIL
FINASTERIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72934-4074	72934-4074-8

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MINOXIDIL	5965120SH1	ACTIB
FINASTERIDE	57GNO57U7G	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
8861f646-2de1-e95c-e053-2a95a90a2041			8861f646-2de0-e95c-e053-2a95a90a2041	2019-05-08	Adverse reactions	Exact identifier spl id: 8861f646-2de1-e95c-e053-2a95a90a2041 spl set id: 8861f646-2de0-e95c-e053-2a95a90a2041

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.