FDA.reportPublic FDA data

Gold Cosmetics Bleach Cream

Manufacturer
Peer Pharm Ltd
Effective date
2017-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:00

Label at a glance#

ProductGold Cosmetics Bleach Cream
Active ingredientHYDROQUINONE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hydroquinone 5%

OTC - PURPOSE SECTION

Face cream for gradual fading of dark spots

INDICATIONS & USAGE SECTION

Face cream for gradual fading of dark spots

Apply a very thin layer once a day, only at night, all over the face

DOSAGE & ADMINISTRATION SECTION

Apply a very thin layer once a day, only at night, all over the face​

WARNINGS SECTION

Warnings:

  • For external use only
  • Avoid contact with eyes
  • If contact occurs, rinse eyes thoroughly with water

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gold Cosmetics Bleach CreamGold Cosmetics Bleach Cream

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
69435-1705-12021-01-29C16284748780-1ba0f9c33-371a-a910-e053-dadaa90a0b85Bleach Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69435-1705-1Gold Cosmetics Bleach Cream30 mg in 1 TUBECREAM302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69435-1705GOLD COSMETICS BLEACH CREAM (HYDROQUINONE CREAM) CREAM [PEER PHARM LTD]2Legacy NDC, 1 package rows20171116_52672cf9-bd14-32e5-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69435-170569435-1705-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETOSTEARYL ALCOHOL2DMT128M1SIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CETEARETH-301R9DCZ5FOXIACT
STEARETH-2153J3F32P58IACT
STEARETH-2V56DFE46J5IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CHLORPHENESINI670DAL4SZIACT
CETYL ALCOHOL936JST6JCNIACT
ALLANTOIN344S277G0ZIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
JOJOBA OIL724GKU717MIACT
DECYL OLEATEZGR06DO97TIACT
SODIUM DITHIONATERPF7Z41GAWIACT
XANTHAN GUMTTV12P4NEEIACT
HYDROQUINONEXV74C1N1AEACTIB
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
WATER059QF0KO0RIACT

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
5e1a9769-16be-1f39-e053-2991aa0a65e052672cf9-bd14-32e5-e054-00144ff8d46c2017-11-16WarningsExact identifier
spl id: 5e1a9769-16be-1f39-e053-2991aa0a65e0
spl set id: 52672cf9-bd14-32e5-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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