FDA.reportPublic FDA data

MINOXIDIL 7% / PROGESTERONE 0.1%

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#

ProductMINOXIDIL 7% / PROGESTERONE 0.1%
Active ingredientMINOXIDIL, PROGESTERONE
Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

cc

Sincerus Florida, LLC adverse reactions.

ADVERSE REACTIONS SECTION

zz

Active, inactive

COMPONENTS

cc

NDC 72934-4748-8 MINOXIDIL 7% / PROGESTERONE 0.1% Solution 60gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

dd

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b46148e2-ee15-98d5-12f0-f5ec8745f6fcProduct name320220927
76820076-f087-4073-b1d1-aa04b361335eProduct name220220921
d3229c1a-4e51-4e04-9b13-00d24fd35242Product name120200821
213f0591-95c1-b398-40b7-08b31f66b026Product name420190206
85b2d644-53b2-f2dc-4dbc-859116ce56c0Product name120140508
d048f0e3-3c40-8816-8c5c-0ca5cd189aacProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-4748-82021-01-29C16284748780-1ba0f9c33-54c8-a910-e053-dadaa90a0b85MINOXIDIL 7% / PROGESTERONE 0.1%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-4748-8MINOXIDIL 7% / PROGESTERONE 0.1%60 g in 1 BOTTLE, GLASSSOLUTION601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-4748MINOXIDIL 7% / PROGESTERONE 0.1% SOLUTION [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20190501_8747e14a-9838-bdcc-e053-2995a90adc35.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72934-4748-8GM - Gram72934-474821fa2c4b-3e24-4f9f-8410-98a607686cc212020-03-10

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
72934-474872934-4748-8

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
PROGESTERONE4G7DS2Q64YACTIB

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
8747e14a-9839-bdcc-e053-2995a90adc358747e14a-9838-bdcc-e053-2995a90adc352019-04-24Adverse reactionsExact identifier
spl id: 8747e14a-9839-bdcc-e053-2995a90adc35
spl set id: 8747e14a-9838-bdcc-e053-2995a90adc35

Reported adverse events (FAERS/openFDA)#

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