FDA.reportPublic FDA data

141030 HYDROQUINONE 8%

Manufacturer
Sincerus Florida, LLC
Effective date
2020-07-02
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:33:04

Label at a glance#

Product141030 HYDROQUINONE 8%
Active ingredientHYDROQUINONE
Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

XX

Sincerus Florida, LLC adverse reactions

ADVERSE REACTIONS SECTION

jj

Active, inactive

COMPONENTS

ss

NDC 72934-6229-2 141030 HYDROQUINONE 8% emulsion 30 gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sfsf

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-6229-22022-01-28C16284748780-1d6a99b39-dd93-a426-e053-dadaa90af4c2141030 HYDROQUINONE 8%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-6229-2141030 HYDROQUINONE 8%30 g in 1 BOTTLE, PUMPEMULSION301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-6229141030 HYDROQUINONE 8% EMULSION [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20200703_a97c133f-f19b-70a4-e053-2995a90a0bbd.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72934-622972934-6229-2

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
HYDROQUINONEXV74C1N1AEACTIB

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
a97c133f-f19c-70a4-e053-2995a90a0bbda97c133f-f19b-70a4-e053-2995a90a0bbd2020-07-02Adverse reactionsExact identifier
spl id: a97c133f-f19c-70a4-e053-2995a90a0bbd
spl set id: a97c133f-f19b-70a4-e053-2995a90a0bbd

Reported adverse events (FAERS/openFDA)#

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