FDA.reportPublic FDA data

Kojic Acid Glutathione Cream

Manufacturer
Shenzhenshishengyakeji Co., Ltd.
Effective date
2024-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:50:32

Label at a glance#

ProductKojic Acid Glutathione Cream
Active ingredientNIACINAMIDE, KOJIC ACID, GLUTATHIONE, CAFFEINE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Kojic Acid：1.3 g in 50 g
Glutathione：1.3 g in 50 g
Niacinamide：1.3 g in 50 g
Caffeine：1.3 g in 50 g

OTC - PURPOSE SECTION

Brightening and moisturizing the skin Frecke removal and hydration Skin fimness.

OTC - ASK DOCTOR SECTION

Conditon worse or doesnot improve after regular use as directed

DOSAGE & ADMINISTRATION SECTION

1.Clean skin completely and dry first
2.Take an appropriate amourt of this product and apply it evenly on the facial skin
3.Massage genily until completely absorbed

OTC - WHEN USING SECTION

Please clean your hands before use to ensure the best results from the product.

WARNINGS SECTION

Please keep out of reach of ohlldren.Do not swallow.Please clean your
hands before use to ensure the best results from the product.Discontinte
usef signs of iritaton or rash oocur.Store in a cool and dry place.

INDICATIONS & USAGE SECTION

Brightening and moisturizing the skin Frecke removal and hydration Skin fimness.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children.

INACTIVE INGREDIENT SECTION

Water:35 g in 50 g
Mineral Oil：6.9 g in 50 g
Ethylhexyl Palmitate：2.8 g in 50 g
Stearyl Alcohol ：2.6 g in 50 g
Glycereth-26：1.8 g in 50 g
Dimethicone：1.85 g in 50 g
PEG-20 Stearate：1.85 g in 50 g
Vitamin E：1.3 g in 50 g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50g50g

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84752-020KOJIC ACID GLUTATHIONE CREAM LOTION/SHAMPOO [SHENZHENSHISHENGYAKEJI CO., LTD.]1Unmatched20241104_25fa32e6-5bac-a337-e063-6394a90a4158.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84752-02084752-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINERAL OILT5L8T28FGPIACT
ETHYLHEXYL PALMITATE2865993309IACT
DIMETHICONE92RU3N3Y1OIACT
NIACINAMIDE25X51I8RD4ACTIB
WATER059QF0KO0RIACT
GLYCERETH-26NNE56F2N14IACT
KOJIC ACID6K23F1TT52ACTIB
GLUTATHIONEGAN16C9B8OACTIB
CAFFEINE3G6A5W338EACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
PEG-20 STEARATENBX892EA57IACT

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
25fa32e6-5bad-a337-e063-6394a90a415825fa32e6-5bac-a337-e063-6394a90a41582024-11-02WarningsExact identifier
spl id: 25fa32e6-5bad-a337-e063-6394a90a4158
spl set id: 25fa32e6-5bac-a337-e063-6394a90a4158

Reported adverse events (FAERS/openFDA)#

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