FDA.reportPublic FDA data

MINOXIDIL 7% / NIACINAMIDE 4%

Manufacturer
Sincerus Florida, LLC
Effective date
2019-05-09
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:28:39

Label at a glance#

ProductMINOXIDIL 7% / NIACINAMIDE 4% s
Active ingredientMINOXIDIL, NIACINAMIDE
Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

eded

Sincerus Florida, LLC. Adverse reactions

ADVERSE REACTIONS SECTION

xxxx

Active, inactive

COMPONENTS

caca

NDC 72934-4147-8. MINOXIDIL 7% / NIACINAMIDE 4%. Solution 60 gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sfsf

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-4147-82021-01-29C16284748780-1ba0f9c33-4feb-a910-e053-dadaa90a0b85MINOXIDIL 7% / NIACINAMIDE 4%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-4147-8MINOXIDIL 7% / NIACINAMIDE 4%s60 g in 1 BOTTLE, PUMPSOLUTION601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-4147MINOXIDIL 7% / NIACINAMIDE 4% S (MINOXIDIL 7% / NIACINAMIDE 4%) SOLUTION [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20190510_8875a838-5aa3-3407-e053-2a95a90ae3eb.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72934-414772934-4147-8

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
MINOXIDIL5965120SH1ACTIB
NIACINAMIDE25X51I8RD4ACTIB

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
8875a838-5aa4-3407-e053-2a95a90ae3eb8875a838-5aa3-3407-e053-2a95a90ae3eb2019-05-09Adverse reactionsExact identifier
spl id: 8875a838-5aa4-3407-e053-2a95a90ae3eb
spl set id: 8875a838-5aa3-3407-e053-2a95a90ae3eb

Reported adverse events (FAERS/openFDA)#

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