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Drug Facts

Manufacturer
Allure Labs, Inc.
Effective date
2010-07-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:22

Label at a glance#

ProductImage MD Lightening Rx
Active ingredientHYDROQUINONE
Label structure6 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

INDICATIONS AND USAGE SECTION:

For Physician Dispensary Only


An effective lightening creme that diminish facial and body discolorations.


DIRECTIONS:

Apply to affected areas in the evening. Apply a sunblock during the day, or as directed by a physician.

Paraben-free

Contains Vitamin C and E

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:

Hydroquinone 4%

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:

Water, Glyceryl Monostearate, Polyoxyl 100 Stearate, Butylene Glycol, Stearyl Alcohol, Stearic Acid, Caprylic and Capric Triglyceride, Linoleic Acid, Soy Phospholipids, Dimethicone, C12-15 Alkyl Benzoate, Xanthan Gum, Magnesium Aluminum Silicate, Cetyl Alcohol, Stearyl Alcohol, Glycerin, Licorice, Phenoxyethanol, Ethylhexylglycerin, Hexylene Glycol, Lactic Acid, Disodium EDTA, Dipotassium Glycyrrizinate, Vitamin E, Sodium Metabisulfite, Fragrance-Orange.

WARNINGS SECTION

WARNING:

For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DISTRIBUTOR:

Image International

Palm Beach, FL 33411 USA


IMAGE OF PRINCIPAL DISPLAY PANEL:

Image of the product: IMAGE MD Lightening Ceme Rx
Image of the product: IMAGE MD Lightening Ceme Rx

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
197795hydroquinone 4 % Topical CreamPSN1
197795hydroquinone 40 MG/ML Topical CreamSCD1
197795hydroquinone 4 % Topical CreamSY1

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
62742-4046-12019-10-21C16284748780-1956f9ecf-c576-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62742-4046-1Image MD Lightening Rx29.6 mL in 1 TUBECREAM29.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62742-4046IMAGE MD LIGHTENING RX (HYDROQUINONE ) CREAM [ALLURE LABS, INC.]1Legacy NDC, 1 package rows20100729_ccb7af09-1957-4305-b1b7-495da3ddb1af.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HYDROQUINONEACTIVE INGREDIENTXV74C1N1AE1
HYDROQUINONEACTIVE MOIETYXV74C1N1AE1

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
62742-404662742-4046-1

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
e379ec77-67e5-4867-9f91-b2add725aa16ccb7af09-1957-4305-b1b7-495da3ddb1af2010-07-29WarningsExact identifier
spl id: e379ec77-67e5-4867-9f91-b2add725aa16
spl set id: ccb7af09-1957-4305-b1b7-495da3ddb1af

Reported adverse events (FAERS/openFDA)#

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