FDA.reportPublic FDA data

KNUCKLEPEELINGBODYOIL

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#

ProductKNUCKLEPEELINGBODYOIL
Active ingredientKOJIC ACID, ALPHA-ARBUTIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

For Body Joint whitening, Spot Removal, moisturizing

INACTIVE INGREDIENT SECTION

AQUA，PROPYLENE GLYCOL，GLYCERETH-26，PENTAERYTHRITYL，TETRAETHYLHEXANOATE，ETHYLHEXYL PALMITATE，GLYCERIN，CETEARYL ALCOHOL，HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE，COPOLYMER，DMDM HYDANTOIN，XANTHAN GUM，AROMA，CETEARYL，GLUCOSIDE，DISODIUM EDTA，GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER，SORBITAN ISOSTEARATE，POLYSORBATE 60，BUTYLENEGLYCOL，1,2-HEXANEDIOL，IODOPROPYNYL BUTYLCARBAMATE，PVM/MA COPOLYMER，PEG-90M

WARNINGS SECTION

Warning.
1、For external use only, avoid contact with eyes when used
2、Keep out of reach of children

INDICATIONS & USAGE SECTION

Whitening, remove dark spots, even skin tone, remove pigmentation.

DOSAGE & ADMINISTRATION SECTION

Knees, Knuckles, and Elbow Lightening body oil is to help reduce the look of unwanted pigmentation, discoloration, dark spots, scars etc. It will minimize the appearance of dull, uneven skin tone and is formulated with natural plant and fruit extracts to safely and effectively revitalize and clarify for radiance and luminosity.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Alpha Arbutin0.5%
KOJIC ACID2%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Active Ingredients
Alpha Arbutin0.5%
KOJIC ACID2%

Uses：
For Body Joint whitening, Spot Removal, moisturizing
The storage method：
Store sealed in a cool place and out of sunlight

Warning.
1、For external use only, avoid contact with eyes when used
2、Keep out of reach of children

Inactive ingredients：
AQUA，PROPYLENE GLYCOL，GLYCERETH-26，PENTAERYTHRITYL，TETRAETHYLHEXANOATE，ETHYLHEXYL PALMITATE，GLYCERIN，CETEARYL ALCOHOL，HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE，COPOLYMER，DMDM HYDANTOIN，XANTHAN GUM，AROMA，CETEARYL，GLUCOSIDE，DISODIUM EDTA，GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER，SORBITAN ISOSTEARATE，POLYSORBATE 60，BUTYLENEGLYCOL，1,2-HEXANEDIOL，IODOPROPYNYL BUTYLCARBAMATE，PVM/MA COPOLYMER，PEG-90M

5DSM2165DSM216

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84423-065-01KNUCKLEPEELINGBODYOIL125 mL in 1 BOTTLE, GLASSCREAM, AUGMENTED1251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84423-065KNUCKLEPEELINGBODYOIL CREAM, AUGMENTED [GUANGZHOU KADIYA BIOTECHNOLOGY CO., LTD.]11 package rows20250226_2e516254-fbc9-1a46-e063-6294a90a64fc.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
84423-06584423-065-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
PENTAERYTHRITYL TETRAETHYLHEXANOATEXJ7052W897IACT
AQUA059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
1,3-BUTYLENEGLYCOL DIMETHACRYLATEOL56191M6NIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
ETHYLHEXYL PALMITATE2865993309IACT
DMDM HYDANTOINBYR0546TOWIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
GLYCERETH-26NNE56F2N14IACT
KOJIC ACID6K23F1TT52ACTIB
PEG-90MRU64142H6PIACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
POLYSORBATE 60CAL22UVI4MIACT
GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER (300000 CP AT 2%)MEA9KH24QGIACT
ALPHA-ARBUTIN72VUP07IT5ACTIB
KOJIC DIPALMITATE13N249RWTMIACT
EDETATE DISODIUM7FLD91C86KIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
CETEARYL ALCOHOL2DMT128M1SIACT
METHYL VINYL ETHER AND MALEIC ANHYDRIDE COPOLYMER (1100000 WAMW)T0VRI38HB0IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT

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
2e516254-fbca-1a46-e063-6294a90a64fc2e516254-fbc9-1a46-e063-6294a90a64fc2025-02-17WarningsExact identifier
spl id: 2e516254-fbca-1a46-e063-6294a90a64fc
spl set id: 2e516254-fbc9-1a46-e063-6294a90a64fc

Reported adverse events (FAERS/openFDA)#

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