HYDRO-Q ® (Hydroquinone 4%) Gel

Manufacturer
Dermavance Pharmaceuticals | Medical Products Laboratories, Inc.
Effective date
2023-01-12
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 20:46:13

Label at a glance#

ProductHydro-Q
Active ingredientHydroquinone
Label structure15 sections

Indications and uses

HYDRO-Q ® is indicated for the gradual bleaching of hyperpigmented skin conditions such as chlosma, melasma, freckles, senile lentigines and areas of melanin hyperpigmentation.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

RX Only

FOR EXTERNAL USE ONLY

DESCRIPTION SECTION

HYDRO-Q® contains hydroquinone USP 4%. Hydroquinone is 1, 4-Benzenediol {CAS 123-31-91}. Hydroquinone is structurally related to monobenzone. Hydroquinone occurs as fine white needles. The drug is freely soluble in water and in alcohol and has a pKa of 9.96. Chemically, hydroquinone is designated as p-dihydroxybenzene; the empirical formula is C6H6O2; The molecular weight is 110.1. The structural formula is:

Chemical Structure
Chemical Structure

ACTIVE INGREDIENT

SPL UNCLASSIFIED SECTION

Hydroquinone USP 4%

OTHER INGREDIENTS: Purified water, Carbomer 940, Sodium Metabisulfite, Sodium Hydroxide, Methylparaben, Edetate Disodium.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Topical application of hydroquinone produces a reversible depigmentation of the skin by inhibition of the enzymatic hydroquinone. oxidation of tyrosine to 3, 4-dihydroxyphenylalanine (dopa) 1 and suppression of other melanocyte metabolic processes. Exposure to sunlight or ultraviolet light will cause regimentation of the bleached areas.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

HYDRO-Q® is indicated for the gradual bleaching of hyperpigmented skin conditions such as chlosma, melasma, freckles, senile lentigines and areas of melanin hyperpigmentation.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

HYDRO-Q® is contraindicated in any patient that has a prior history of sensitivity or allergic reaction to hydroquinone or any of the other ingredients. The safety of topical hydroquinone use during pregnancy or in children (12 years and under) has not been established.

WARNINGS

WARNINGS SECTION

  1. CAUTION: Hydroquinone is a depigmenting agent that may produce unwanted cosmetic effects if not used as directed. The physician should be familiar with the contents of this insert before prescribing or dispensing this medication.
  2. Test for skin sensitivity before using HYDRO-Q® by applying a small amount of the gel to an unbroken patch of skin and check within 24 hours. Minor redness is not a contraindication but where there is itching and vesicle formation or excessive inflammatory response further treatment is not advised. Close patient supervision is recommended. Contact with the eyes should be avoided. If no lightening effect is noted after 2 months of treatment the use of HYDRO-Q® should be discontinued. HYDRO-Q® is formulated for the treatment of dyschromia and should not be used for the prevention of sunburn.
  3. Sunscreen use is an essential aspect of hydroquinone therapy because even minimal sunlight sustains melanocytic activity. To prevent repigmentation during treatment and maintenance therapy, sun exposure on treated skin should be avoided by application of a broad spectrum sunscreen SPF 15 or greater) or by use of protective clothing
  4. Keep this and all medications out of reach of children. In case of accidental ingestion, contact a physician or a poison control center immediately.
  5. WARNING: Contains sodium metabisulfite, a sulfite that may cause serious allergic reactions (e.g., hives, itching, wheezing, anaphylaxis, severe asthma attack) in certain susceptible persons
  6. On rare occasions, a gradual blue-black darkening of the skin may occur, in which case, use of HYDRO-Q® should be discontinued and a physician contacted immediately

PRECAUTIONS

PRECAUTIONS SECTION

A. Pregnancy Category C

PREGNANCY SECTION

Animal reproduction studies have not been conducted with topical hydroquinone. It is also not known whether hydroquinone can cause fetal harm when used topically on a pregnant woman, or can affect reproductive capacity.

B. Nursing mothers

NURSING MOTHERS SECTION

It is not known whether topical hydroquinone is absorbed or excreted in human milk. Caution is advised when used by a nursing mother.

C. Pediatric usage

PEDIATRIC USE SECTION

Safety and effectiveness in pediatric patients below the age of 12 years have not been established.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

No systemic reactions have been reported. Occasional cutaneous hypersensitivity (localized contact dermatitis) may occur, in which case the medication should be discontinued and the physician notified immediately

OVERDOSAGE

OVERDOSAGE SECTION

There have been no systemic reactions reported from the use of topical hydroquinone. However, treatment should be limited to relatively small areas of the body at one time, since some patients experience a skin reddening and a mild burning sensation that does not preclude treatment

DOSAGE AND ADMINSTRATION

DOSAGE & ADMINISTRATION SECTION

HYDRO-Q® should be applied to the affected areas twice daily, morning and before bedtime or as directed by a physician.

During and after the use of HYDRO-Q®, sun exposure should be limited and a sunscreen agent or protective clothing should be used to cover up the treated areas to prevent regimentation. If no lightening effect is noted after two months of treatment, use of HYDRO-Q® should be discontinued. There is no recommended dosage for children under the age of 12 years of age except under the advice and supervision of a physician.

HOW SUPPLIED

HOW SUPPLIED SECTION

HYDRO-Q® (Hydroquinone 4%) Gel is supplied in a 30 g tube.

NDC: 30815-0040-1

STORAGE AND HANDLING SECTION

Store at controlled room temperature, between 15° and 30°C (59°and 86°F).

REFERENCES

REFERENCES SECTION

  1. Denton C, Fitzpatrick TB, Lerner AB. Inhibition of melanin formation by chemical agents. J Invest Dermatology. 1952; 18: 119-135.
  2. Fitzpatrick TB, Jimbow K, Obata M, Panthak M. Mechanism of depigmentation by hydroquinone. J Invest Dermatology. 1974; 62: 436-449.
  3. Anderson RR, Parrish JA, Pitts D, Urbach F. UVA, Biological Effects of Ultraviolet Radiation With Emphasis on Human Responses to Longwave Ultraviolet. New York and London: Plenum Press; 1978: 151.

SPL UNCLASSIFIED SECTION

Distributed by:
DermAvance Pharmaceuticals, Malvern, PA 19355
NDC 30815-0040-1

P15132917-1

I2430214

PRINCIPAL DISPLAY PANEL - 30 g Tube Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 30815-0040-1

Rx Only

HYDRO-Q 4% GEL®

(Hydroquinone 4%) Gel®

SKIN BLEACHING GEL

DermAvance®
Advanced Skin Care
www.DermAvance.com

30 g

PRINCIPAL DISPLAY PANEL - 30 g Tube Box
PRINCIPAL DISPLAY PANEL - 30 g Tube Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
310926hydroquinone 4 % Topical GelPSN4
310926hydroquinone 0.04 MG/MG Topical GelSCD4
310926hydroquinone 4 % Topical GelSY4

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30815-0040-1Hydro-Q1 in 1 BOXGEL14
30815-0040-1Hydro-Q30 g in 1 TUBEGEL304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30815-0040HYDRO-Q (HYDROQUINONE) GEL [DERMAVANCE PHARMACEUTICALS]4Current NDC, Legacy NDC, 2 package rows20230113_486781be-498a-49b4-9a80-2dfd02f5e358.zip

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30815-004030815-0040-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
Hydro-QHYDROQUINONEDermavance Pharmaceuticals486781be-498a-49b4-9a80-2dfd02f5e3582023-01-12Warnings, Adverse reactionsExact identifier
ndc (package): 30815-0040-1
ndc (product): 30815-0040
ndc11 (package): 30815004001
spl id: c8c85250-96ad-4bd8-9f74-a55737881fd3
spl set id: 486781be-498a-49b4-9a80-2dfd02f5e358

Reported adverse events (FAERS/openFDA)#

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