FDA.reportPublic FDA data

GZE RainbowSoap

Manufacturer
Guangzhou Yilong Cosmetics Co.,Ltd. | Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-08-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:55:58

Label at a glance#

ProductGZE RainbowSoap
Active ingredientKOJIC ACID, ARBUTIN
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Kojic Acid 0.35%

Arbutin 1%

INACTIVE INGREDIENT SECTION

Glycerin

Carica Papaya (Papaya) Fruit Extract

Cocos Nucifera (Coconut) Oil

Elaeis Guineensis (Palm) Oil

Ricinus Communis (Castor) Seed Oil

Carthamus Tinctorus (Safflower) Seed Oil

Aqua

Sorbitol

Sorbitan Oleate

Hydrolyzed Soy Protein

Titanium Dioxide

Fragrance

OTC - PURPOSE SECTION

Cleanser.

INDICATIONS & USAGE SECTION

When using, you can wet the soap and gently rub it with your hands. After foaming,apply it to your body or face, and rinse it with water.

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

When using, you can wet the soap and gently rub it with your hands. After foaming,apply it to your body or face, and rinse it with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-139GZE RAINBOWSOAP (KOJIC ACID,ARBUTIN) SOAP [GUANGZHOU YILONG COSMETICS CO.,LTD.]1Unmatched20240824_2056c8da-c6f3-c8fa-e063-6394a90a994d.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-13983566-139-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
PALM OIL5QUO05548ZIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
COCONUT OILQ9L0O73W7LIACT
RICINUS COMMUNIS SEED7EK4SFN1TXIACT
PEG-6 SORBITAN OLEATE58O7V09UCIIACT
HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW)1394NXB9L6IACT
KOJIC ACID6K23F1TT52ACTIB
CARICA PAPAYA WHOLES0U63B0Q51IACT
SORBITOL506T60A25RIACT
GLYCERINPDC6A3C0OXIACT
FRAGRANCE 135765EM498GW35IACT
ARBUTINC5INA23HXFACTIB
WATER059QF0KO0RIACT
SAFFLOWER OIL65UEH262ISIACT

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
39f69f83-f767-685f-e063-6294a90a02c92056c8da-c6f3-c8fa-e063-6394a90a994d2025-07-15WarningsExact identifier
spl set id: 2056c8da-c6f3-c8fa-e063-6394a90a994d

Reported adverse events (FAERS/openFDA)#

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