FDA.reportPublic FDA data

DEXAMETHASONE SODIUM PHOSPHATE

Manufacturer
Sincerus Florida | 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#

ProductDEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5% / TRETINOIN 0.025%
Active ingredientDEXAMETHASONE SODIUM PHOSPHATE, FINASTERIDE, MINOXIDIL, TRETINOIN
Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

eded

Sincerus Florida, LLC. Adverse reactions

ADVERSE REACTIONS SECTION

adad

Active, Inactive

COMPONENTS

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NDC 72934-4070-8 DEXAMETHASONE SODIUM PHOSPHATE USP 0.1% / FINASTERIDE USP 0.1% / MINOXIDIL USP 5% / TRETINOIN USP 0.025%. Solution 60 gm.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

zczc

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b80ad7bc-1b6f-7ef4-1ed0-86cd9f459d60Product name620251124
1426d8f8-b7d5-4053-8554-613df00c0d86Product name220250616
0e7b8bf1-c46c-4de6-b26a-0c50e34364ecProduct name220250521
1ea46721-9071-6b81-fd0a-a82bfbb014ecProduct name720250220
525701df-f985-480d-995a-e0ee70c2bdf4Product name520250128
ea50b939-d92a-4100-84f5-1c1089663837Product name220240705
e3af9708-3004-7392-4046-5311eaa8bab5Product name320221128
941f67d9-7f03-56d2-750c-36de24f654dbProduct name320221117
928d249c-35c3-4d88-a9ef-cf2f2e31b96fProduct name120220706
d7d46a10-8766-d3c8-ebf2-2ccd9efdcae8Product name220220506
7b2c58e8-5850-4e3e-82e9-b1593b1de761Product name520220210
13e7e7e3-e885-4c79-af6d-dad1aedbb06eProduct name120220128
81e34474-b0a5-434f-8104-25d689efc99eProduct name120200303
05ab9c01-cd9a-4f59-b2e8-ddcb887cac39Product name120190408
503b047e-e62d-4745-9011-522b13bc701bProduct name120181206
0c7dba41-c919-5809-508d-4affe6cfcff2Product name220170817
d00474ae-23eb-a8eb-bf56-520e590cc6dbProduct name220170406
0f90664c-9d0e-f046-dc6a-73563cd8347eProduct name220170405
7d41caa2-0b5d-9b03-ab8d-84271de26ef4Product name220170314
50ca9ff5-82dd-9971-4f2c-5845a76a8572Product name220150818
0a8118e4-08c6-b395-9ddc-d3e425e0493aProduct name120140508
233bcb0a-cf40-b0a1-b346-c83ac2f43579Product name120140508
399647c0-db89-02d1-991c-0c17b584482cProduct name120140508
3e9a6377-704f-dff7-b19f-56c98d40c444Product name120140508
4d2e6ff9-14f5-b84f-c39b-373b005712c1Product name120140508
725d71bf-f956-5cad-e556-fa39cb060dc8Product name120140508
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508
9ea85abb-fa68-5da6-ab60-2c7eef579000Product name120140508
d029211e-5e6b-725f-3696-ac6ff77da222Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-4070-82021-01-29C16284748780-1ba0f9c33-26f8-a910-e053-dadaa90a0b85DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5% / TRETINOIN 0.025%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-4070-8DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5% / TRETINOIN 0.025%60 g in 1 BOTTLE, GLASSSOLUTION601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-4070DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5% / TRETINOIN 0.025% SOLUTION [SINCERUS FLORIDA]1Legacy NDC, 1 package rows20190509_88612151-53b2-b592-e053-2995a90a0025.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72934-407072934-4070-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
DEXAMETHASONE SODIUM PHOSPHATEAI9376Y64PACTIR
FINASTERIDE57GNO57U7GACTIB
MINOXIDIL5965120SH1ACTIB
TRETINOIN5688UTC01RACTIB

Source Document#

Source XML · Source PDF

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
88612151-53b3-b592-e053-2995a90a002588612151-53b2-b592-e053-2995a90a00252019-05-08Adverse reactionsExact identifier
spl id: 88612151-53b3-b592-e053-2995a90a0025
spl set id: 88612151-53b2-b592-e053-2995a90a0025

Reported adverse events (FAERS/openFDA)#

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