FDA.reportPublic FDA data

GZE AHA Body Lotion

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-07-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:57:53

Label at a glance#

ProductGZE AHA BodyLotion
Active ingredientARBUTIN, CITRIC ACID, 1-STEARYL ESTER
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Citric acid 1%

Arbutin 1%

INACTIVE INGREDIENT SECTION

Water

Cyclopentasiloxane

Dimethicone

Glycerin

Diethylhexyl Carbonate

Titanium Dioxide

Butylene Glycol

C12-15 Alkyl Benzoate

Polymethylsilsesquioxane

Polyglyceryl-4Diisostearate/

Polyhydroxystearate/Sebacate

Ethylhexyl Methoxycinnamate

Cetyl PEG/PPG-10/1Dimethicone

Imidazolidinyl Urea

Benzophenone-3

Cetearyl Dimethicone Crosspolymer

Sodium Chloride

Hydrolyzed Extensin

Phospholipids

Parfum

Phenoxyethanol

Glutathione

Niacinamide

Betaine

OTC - PURPOSE SECTION

Softens old body cuticles.

INDICATIONS & USAGE SECTION


Apply over your body daily in the morning and before bed.

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


Apply over your body daily in the morning and before bed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-002GZE AHA BODYLOTION (ARBUTIN,CITRIC ACID) LOTION [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20240731_1e6ea57a-b02b-b399-e063-6294a90a3a15.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-00283566-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIETHYLHEXYL CARBONATEYCD50O0Z6LIACT
C12-20 ALKYL BENZOATEY15I6XI14CIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
SODIUM CHLORIDE451W47IQ8XIACT
BETAINE3SCV180C9WIACT
ARBUTINC5INA23HXFACTIB
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
N-(1,3,4-TRIS(HYDROXYMETHYL)-2,5-DIOXO-4-IMIDAZOLIDINYL)-N,N'-BIS(HYDROXYMETHYL)UREAENL2IA4WGWIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
PARFUMIDINEA2Q2LHC6MAIACT
PENTAMETHYL CYCLOPENTASILOXANEK29QC5YCW8IACT
OXYBENZONE95OOS7VE0YIACT
EGG PHOSPHOLIPIDS1Z74184RGVIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER4ZK9VP326RIACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)V2W71V8T0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYMETHYLSILSESQUIOXANE (11 MICRONS)Z570VEV8XKIACT
CITRIC ACID, 1-STEARYL ESTERE945AJ51FAACTIB
GLYCERINPDC6A3C0OXIACT
GLUTATHIONEGAN16C9B8OIACT
NIACINAMIDE25X51I8RD4IACT

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
39f5cf9c-276c-93bf-e063-6394a90ac5d91e6ea57a-b02b-b399-e063-6294a90a3a152025-07-15WarningsExact identifier
spl set id: 1e6ea57a-b02b-b399-e063-6294a90a3a15

Reported adverse events (FAERS/openFDA)#

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