Advanced Dual Complex Fade Gel Maximum Strength Plus

Manufacturer
Biocosmetic Research Labs
Effective date
2009-02-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:25:18

Label at a glance#

ProductAdvanced Dual Complex Fade Maximum Strength Plus
Active ingredientHydroquinone
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


Active Ingredient:

Hydroquinone 2%

OTC - PURPOSE SECTION


Purpose:

Skin Lightening Gel

INDICATIONS & USAGE SECTION


Uses:

For gradual fading of dark (brownish) spots

WARNINGS SECTION


Warnings:

Avoid contact with eyes.  Children under 12 years of age; Do not use unless directed by a doctor.

OTC - STOP USE SECTION

Some users may experience a mild irritation. If skin irritation becomes severe, stop use and consult a doctor.

DOSAGE & ADMINISTRATION SECTION


Directions:

Apply a small amount as a thin layer on the affected area or use as directed by a doctor.  Sun exposure should be limited by using a sunscreen agent or a sun blocking agent.

INACTIVE INGREDIENT SECTION


Other Ingredients:

Water, Propylene Glycol, Carbomer, Sodium Palmitoyl Proline, Nymphaea Alba Flower Extract, glycerin, Citrus Unshiu Peel Extract, Sodium Hydroxymethylglycinate,Sodium Sulfite, Sodium Metabisulfite, Butylene Glycol, Phenoxyethanol, Disodium EDTA, Polysorbate 20, Trisodium EDTA, Benzophenone-4, EDTA, Caprylyl Glycol, Hexylene Glycol, Sodium Hydroxide, Caramel, Mica, Iron Oxides (CI 77491)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton AdvancedfadegelmaxImage of carton Advancedfadegelmax

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
199176hydroquinone 2 % Topical GelPSN3
199176hydroquinone 0.02 MG/MG Topical GelSCD3
199176hydroquinone 2 % Topical GelSY3

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
59735-310-282020-01-31C16284748780-19d75b9d0-e0f8-f424-e053-dadaa90a57ceAdvanced Dual Complex Fade Gel Maximum Strength Plus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59735-310-28Advanced Dual Complex FadeMaximum Strength Plus28.4 g in 1 BOTTLE, PUMPGEL28.43
59735-310-28Advanced Dual Complex FadeMaximum Strength Plus1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59735-310ADVANCED DUAL COMPLEX FADE MAXIMUM STRENGTH PLUS (HYDROQUINONE) GEL [BIOCOSMETIC RESEARCH LABS]3Legacy NDC, 2 package rows20100722_6890a8c7-5561-4a39-bb77-f72ba7692879.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HydroquinoneACTIVE INGREDIENTXV74C1N1AE3
HydroquinoneACTIVE MOIETYXV74C1N1AE3

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
59735-31059735-310-28

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
fed097e8-f13e-411b-b54c-5a7b0f433c846890a8c7-5561-4a39-bb77-f72ba76928792009-02-25WarningsExact identifier
spl id: fed097e8-f13e-411b-b54c-5a7b0f433c84
spl set id: 6890a8c7-5561-4a39-bb77-f72ba7692879

Reported adverse events (FAERS/openFDA)#

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