FDA.reportPublic FDA data

Super Lightening Based on Gold 24k and Kojic Acid Cream

Manufacturer
Guangzhou Kadiya Biotechnology Co., Ltd.
Effective date
2025-02-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:55:51

Label at a glance#

ProductSuper Lightening Based on Gold 24k and Kojic Acid Cream
Active ingredientKOJIC ACID, GLUTATHIONE, NIACINAMIDE, SALICYLIC ACID, ALPHA-ARBUTIN, TOCOPHEROL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

For Facial Skin Moisturizing, Antioxidant, Blemish Removal, Whitening, Brightening

INACTIVE INGREDIENT SECTION

AQUA，MINERAL OIL，GLYCERIN，Polyethylene，PROPYLENE GLYCOL，STEARYL ALCOHOL，BUTYLENE GLYCOL，Steareth-2，Steareth-21，CETYL ALCOHOL，DIMETHICONE，Isosorbide Dimethyl Ether，GLYCERYL STEARATE，PEG-100，PHENOXYETHANOL，ALLANTOIN，Polyacrylamide，ALOE BARBADENSIS LEAF EXTRACT，ANTHEMIS NOBILIS FLOWER EXTRACT，PORTULACA OLERACEA FLOWER/LEAF/STEM EXTRACT，PELARGONIUM GRAVEOLENS FLOWER/LEAF/STEM EXTRACT，XANTHAN GUM，FRAGRANCE，ETHYLHEXYLGLYCERIN， C13-14 Isoparaffin，DISODIUM EDTA，Laureth-7

WARNINGS SECTION

Warning.
1.Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2、For external use only, avoid contact with eyes when used
3、Keep out of reach of children

INACTIVE INGREDIENT SECTION

Extreme Shine face cream will lighten your skin thanks to Kojic acid which is effective as a complexion and pigment spot corrector

DOSAGE & ADMINISTRATION SECTION

On previously cleansed skin, apply your extreme shine face cream morning and evening, visible results after 7 days of use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
NIACINAMIDE0.5%
KOJIC ACID 1%
SALICYLIC ACID0.5%
GLUTATHIONE 0.5%
ALPHA-ARBUTIN1%
TOCOPHEROL1%

INDICATIONS & USAGE SECTION

Extreme Shine face cream will lighten your skin thanks to Kojic acid which is effective as a complexion and pigment spot corrector. 24K gold will help you fight the effects of aging will smooth your skin and make it more radiant.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NIACINAMIDE0.5%
KOJIC ACID 1%
SALICYLIC ACID0.5%
GLUTATHIONE 0.5%
ALPHA-ARBUTIN1%
TOCOPHEROL1%

Uses：
For Facial Skin Moisturizing, Antioxidant, Blemish Removal, Whitening, Brightening
The storage method：
Store sealed in a cool place and out of sunlight

Warning.
1.Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2、For external use only, avoid contact with eyes when used
3、Keep out of reach of children

Inactive ingredients：
AQUA，MINERAL OIL，GLYCERIN，Polyethylene，PROPYLENE GLYCOL，STEARYL ALCOHOL，BUTYLENE GLYCOL，Steareth-2，Steareth-21，CETYL ALCOHOL，DIMETHICONE，Isosorbide Dimethyl Ether，GLYCERYL STEARATE，PEG-100，PHENOXYETHANOL，ALLANTOIN，Polyacrylamide，ALOE BARBADENSIS LEAF EXTRACT，ANTHEMIS NOBILIS FLOWER EXTRACT，PORTULACA OLERACEA FLOWER/LEAF/STEM EXTRACT，PELARGONIUM GRAVEOLENS FLOWER/LEAF/STEM EXTRACT，XANTHAN GUM，FRAGRANCE，ETHYLHEXYLGLYCERIN， C13-14 Isoparaffin，DISODIUM EDTA，Laureth-7

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84423-068-01Super Lightening Based on Gold 24k and Kojic Acid Cream50 g in 1 BOTTLE, GLASSCREAM, AUGMENTED501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84423-068SUPER LIGHTENING BASED ON GOLD 24K AND KOJIC ACID CREAM CREAM, AUGMENTED [GUANGZHOU KADIYA BIOTECHNOLOGY CO., LTD.]11 package rows20250226_2e52cf9b-cae9-9b54-e063-6394a90a2fbd.zip

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84423-06884423-068-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
AQUA059QF0KO0RIACT
LAURETH-7Z95S6G8201IACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
XANTHAN GUMTTV12P4NEEIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
KOJIC ACID6K23F1TT52ACTIB
GLYCERINPDC6A3C0OXIACT
STEARETH-2V56DFE46J5IACT
DIMETHICONE92RU3N3Y1OIACT
PEG-100TVH7653921IACT
GLYCERYL STEARATE230OU9XXE4IACT
POLYACRYLAMIDE (10000 MW)E2KR9C9V2IIACT
ALLANTOIN344S277G0ZIACT
DIMETHYL ISOSORBIDESA6A6V432SIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
GLUTATHIONEGAN16C9B8OACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
EDETATE DISODIUM7FLD91C86KIACT
ANTHEMIS NOBILIS FLOWER OILUB27587839IACT
PELARGONIUM GRAVEOLENS WHOLE0E553RP62FIACT
NIACINAMIDE25X51I8RD4ACTIB
SALICYLIC ACIDO414PZ4LPZACTIB
ALPHA-ARBUTIN72VUP07IT5ACTIB
MINERAL OILT5L8T28FGPIACT
PORTULACA OLERACEA WHOLED5J3623SV2IACT
CETYL ALCOHOL936JST6JCNIACT
STEARETH-2153J3F32P58IACT
TOCOPHEROLR0ZB2556P8ACTIB
POLYETHYLENEUG00KM4WR7IACT
BUTYLENE GLYCOL3XUS85K0RAIACT

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
2e52cf9b-caea-9b54-e063-6394a90a2fbd2e52cf9b-cae9-9b54-e063-6394a90a2fbd2025-02-17WarningsExact identifier
spl id: 2e52cf9b-caea-9b54-e063-6394a90a2fbd
spl set id: 2e52cf9b-cae9-9b54-e063-6394a90a2fbd

Reported adverse events (FAERS/openFDA)#

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