FDA.reportPublic FDA data

FINASTERIDE 0.1% / MINOXIDIL 7%

Manufacturer
Sincerus Florida, LLC
Effective date
2019-04-24
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:28:27

Label at a glance#

ProductFINASTERIDE 0.1% / MINOXIDIL 7%
Active ingredientFINASTERIDE, MINOXIDIL
Label structure4 sections

Label contents#

Full prescribing information#

Directions for Use

INSTRUCTIONS FOR USE SECTION

cc

Sincerus Florida, LLC adverse reactions

ADVERSE REACTIONS SECTION

ss

Active, inactive

COMPONENTS

gg

NDC 72934-4075-8 FINASTERIDE USP 0.1% / MINOXIDIL USP 7%. Solution 60gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

xx

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
FINASTERIDE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
MINOXIDIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
928d249c-35c3-4d88-a9ef-cf2f2e31b96fProduct name120220706
d00474ae-23eb-a8eb-bf56-520e590cc6dbProduct name220170406
0f90664c-9d0e-f046-dc6a-73563cd8347eProduct name220170405

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-4075-82021-01-29C16284748780-1ba0f9c33-305a-a910-e053-dadaa90a0b85FINASTERIDE 0.1% / MINOXIDIL 7%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-4075-8FINASTERIDE 0.1% / MINOXIDIL 7%60 g in 1 BOTTLE, GLASSSOLUTION601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-4075FINASTERIDE 0.1% / MINOXIDIL 7% SOLUTION [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20190501_8747ab73-38f7-0828-e053-2a95a90a99cd.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72934-4075-8GM - Gram72934-4075dc35b1aa-94df-4f01-b58c-7616a4fe8f8f12020-03-10

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72934-407572934-4075-8

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
NameUNIIKind
FINASTERIDE57GNO57U7GACTIB
MINOXIDIL5965120SH1ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
8747ab73-38f8-0828-e053-2a95a90a99cd8747ab73-38f7-0828-e053-2a95a90a99cd2019-04-24Adverse reactionsExact identifier
spl id: 8747ab73-38f8-0828-e053-2a95a90a99cd
spl set id: 8747ab73-38f7-0828-e053-2a95a90a99cd

Reported adverse events (FAERS/openFDA)#

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