DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5%

Manufacturer
Sincerus Florida, LLC
Effective date
2019-05-10
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:28:41

Label at a glance#

ProductDAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5%
Active ingredientNIACINAMIDE, DAPSONE, SPIRONOLACTONE
Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

dd

Sincerus Florida, LLC. Adverse reactions

ADVERSE REACTIONS SECTION

zz

Active, inactive

COMPONENTS

ss

NDC 72934-1061-2 DAPSONE USP 6% / NIACINAMIDE USP 2% / SPIRONOLACTONE USP 5%. Gel 30gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sfsf

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DAPSONE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
SPIRONOLACTONE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4ae3f83f-9ccb-db71-5718-0b1e959868dfProduct name520260113
d335cba1-5b36-51c8-120a-594ec9d05330Product name520251114
25f5e2cf-3572-477b-994c-aa692751e5a8Product name220250616
5ae2790a-f798-4a69-8811-64a4723c389aProduct name520250325
b8929bfc-0002-d39a-046d-72ddf714efbeProduct name620190618
f151007d-265d-9fbe-857d-1d44f1cb76baProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-1061-22021-01-29C16284748780-1ba0f9c33-2647-a910-e053-dadaa90a0b85DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-1061-2DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5%30 g in 1 BOTTLE, PUMPGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-1061DAPSONE 6% / NIACINAMIDE 2% / SPIRONOLACTONE 5% GEL [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20190511_888b2203-469f-d599-e053-2995a90a7de1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72934-1061-2GM - Gram72934-1061fa87af7f-837e-4d0d-b46b-c5e8f7701ab412020-02-13

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
72934-106172934-1061-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4ACTIB
DAPSONE8W5C518302ACTIB
SPIRONOLACTONE27O7W4T232ACTIB

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
888b2203-46a0-d599-e053-2995a90a7de1888b2203-469f-d599-e053-2995a90a7de12019-05-10Adverse reactionsExact identifier
spl id: 888b2203-46a0-d599-e053-2995a90a7de1
spl set id: 888b2203-469f-d599-e053-2995a90a7de1

Reported adverse events (FAERS/openFDA)#

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