HYDROQUINONE 8%

Manufacturer: Sincerus Florida, LLC | Sincerus Forida, LLC
Effective date: 2019-05-20
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 20:28:51

Label at a glance#

ProductHYDROQUINONE 8%.

Active ingredientHYDROQUINONE

Label structure4 sections

Label contents#

Full prescribing information#

Directions for use.

INSTRUCTIONS FOR USE SECTION

Sincerus Florida, LLC. Adverse reactions

ADVERSE REACTIONS SECTION

Active, inactive

COMPONENTS

sdf

NDC 72934- 6122-2 HYDROQUINONE 8%. Emulsion 30 gm.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
HYDROQUINONE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
85490a6b-2306-6bf2-c51b-eb63537dc2da	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72934-6122-2	2021-01-29	C162847	48780-1	ba0f9c33-3b70-a910-e053-dadaa90a0b85	HYDROQUINONE 8%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72934-6122-2	HYDROQUINONE 8%.	30 g in 1 BOTTLE, PUMP	EMULSION	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72934-6122	HYDROQUINONE 8%. EMULSION [SINCERUS FLORIDA, LLC]	1	Legacy NDC, 1 package rows	20190521_89535686-83e5-20c6-e053-2a95a90a6d84.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72934-6122-2	GM - Gram	72934-6122	7d98597e-bc58-47f2-b41f-6816dc616997	1	2020-03-10

Products#

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

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

HYDROQUINONE 8%.
HYDROQUINONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72934-6122	72934-6122-2

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
Name	UNII	Kind
HYDROQUINONE	XV74C1N1AE	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
89535686-83e6-20c6-e053-2a95a90a6d84			89535686-83e5-20c6-e053-2a95a90a6d84	2019-05-20	Adverse reactions	Exact identifier spl id: 89535686-83e6-20c6-e053-2a95a90a6d84 spl set id: 89535686-83e5-20c6-e053-2a95a90a6d84

Reported adverse events (FAERS/openFDA)#

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