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.
HYDRO-Q ® is indicated for the gradual bleaching of hyperpigmented skin conditions such as chlosma, melasma, freckles, senile lentigines and areas of melanin hyperpigmentation.
RX Only
FOR EXTERNAL USE ONLY
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:

Hydroquinone USP 4%
OTHER INGREDIENTS: Purified water, Carbomer 940, Sodium Metabisulfite, Sodium Hydroxide, Methylparaben, Edetate Disodium.
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.
HYDRO-Q® is indicated for the gradual bleaching of hyperpigmented skin conditions such as chlosma, melasma, freckles, senile lentigines and areas of melanin hyperpigmentation.
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.
See Warnings
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.
It is not known whether topical hydroquinone is absorbed or excreted in human milk. Caution is advised when used by a nursing mother.
Safety and effectiveness in pediatric patients below the age of 12 years have not been established.
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
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
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.
HYDRO-Q® (Hydroquinone 4%) Gel is supplied in a 30 g tube.
NDC: 30815-0040-1
Store at controlled room temperature, between 15° and 30°C (59°and 86°F).
Distributed by:
DermAvance Pharmaceuticals, Malvern, PA 19355
NDC 30815-0040-1
P15132917-1
I2430214
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

| Class | Version | Type | Effective |
|---|---|---|---|
| HYDROQUINONE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 85490a6b-2306-6bf2-c51b-eb63537dc2da | Product name | 1 | 20140508 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 30815-0040-1 | Hydro-Q | 1 in 1 BOX | GEL | 1 | 4 | |
| 30815-0040-1 | Hydro-Q | 30 g in 1 TUBE | GEL | 30 | 4 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 30815-0040 | HYDRO-Q (HYDROQUINONE) GEL [DERMAVANCE PHARMACEUTICALS] | 4 | Current NDC, Legacy NDC, 2 package rows | 20230113_486781be-498a-49b4-9a80-2dfd02f5e358.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 30815-0040 | 30815-0040-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Hydroquinone | XV74C1N1AE | ACTIB |
| Water | 059QF0KO0R | IACT |
| CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | IACT |
| SODIUM METABISULFITE | 4VON5FNS3C | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Hydro-Q | HYDROQUINONE | Dermavance Pharmaceuticals | 486781be-498a-49b4-9a80-2dfd02f5e358 | 2023-01-12 | Warnings, Adverse reactions | 30815-0040-1 30815-0040 30815004001 c8c85250-96ad-4bd8-9f74-a55737881fd3 486781be-498a-49b4-9a80-2dfd02f5e358 |
Adverse event summaries are temporarily unavailable. Other product information remains available.