FDA.reportPublic FDA data

BODY / FACE SUNSCREEN SUN

Manufacturer
Guanghzou AiXin Biotech Co., Ltd
Effective date
2026-03-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:38:01

Label at a glance#

ProductBODY / FACE SUNSCREEN SUN
Active ingredientHOMOSALATE, OCTINOXATE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

1.69 FL.OZ/50 ML

INACTIVE INGREDIENT SECTION

Octisalate,Zinc Oxide,Aloe Barbadensis Leaf (Aloe Vera Gel) Juice,Amodimethicone,Aqua (Deionized Water),Butylene Glycol
Butyloctyl Salicylate,C12-15 Alkyl Benzoate,Camellia Sinensis (Green Teat) Extract,Caprylic/Capric Triglyceride
Carbomer,Citric Acid,Citrullus Lanatus (Watermelon) Extract,Ceramide NG,Cocamidopropyl Betaine,Colloidal Oatmeal
Cyclopentasiloxane,Daucus Carota Sativa (Carrot) Extract,Ferulic Acid, Glycerin,Glyceryl Caprylate,Glyceryl Stearate,
Glyceryl Undecylenate,Hyaluronic Acid,Hydrogenated Methyl Abietate,Hydroxypropyl Cyclodextrin
Leuconostoc/Radish Root Ferment Filtrate,Melaleuca Alternifolia (Tea Tree) Oil,Niacinamide
Palmitoyl Tetrapeptide-7,Palmitoyl Tripeptide-1

OTC - ACTIVE INGREDIENT SECTION

Homosalate,Octinoxate

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

Sunscreen

WARNINGS SECTION

Please put it in a place where children are not in contact

INDICATIONS & USAGE SECTION

Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85897-374-01BODY / FACE SUNSCREEN SUN5 in 1 BOXCREAM, AUGMENTED52
85897-374-01BODY / FACE SUNSCREEN SUN1 in 1 BAGCREAM, AUGMENTED12

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
85897-37485897-374-01

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
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE75D21FL1PIIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
CITRIC ACID2968PHW8QPIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
FERULIC ACIDAVM951ZWSTIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
GLYCERYL STEARATE230OU9XXE4IACT
HYALURONIC ACIDS270N0TRQYIACT
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATED2QHA03458IACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAFG43C57162KIACT
PALMITOYL TETRAPEPTIDE-7Q41S464P1RIACT
ZINC OXIDESOI2LOH54ZIACT
NIACINAMIDE25X51I8RD4IACT
HOMOSALATEV06SV4M95SACTIB
THYMUS VULGARIS (THYME) OIL2UK410MY6BIACT
OCTINOXATE4Y5P7MUD51ACTIB
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
CARBOMER0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PALMITOYL TRIPEPTIDE-38T7A529FB8OIACT
AQUA059QF0KO0RIACT
PENTAMETHYL CYCLOPENTASILOXANEK29QC5YCW8IACT
DAUCUS CAROTA SATIVA (CARROT) SEED OIL595AO13F11IACT
HYDROGENATED METHYL ABIETATEA23O709X8OIACT
CITRULLUS LANATUS (WATERMELON) SEED OILL33J06UQTTIACT
CERAMIDE NGC04977SRJ5IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
CAMELLIA SINENSIS LEAFW2ZU1RY8B0IACT
PALMITOYL TRIPEPTIDE-1RV743D216MIACT
OCTISALATE4X49Y0596WIACT
AMODIMETHICONE (1300 CST)3V7U636DWNIACT

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
BODY / FACE SUNSCREEN SUNBODY / FACE SUNSCREEN SUNGuanghzou AiXin Biotech Co., Ltd39035b99-e560-e6b6-e063-6294a90a19c62026-03-17WarningsExact identifier
ndc (package): 85897-374-01
ndc (product): 85897-374
ndc11 (package): 85897037401
spl id: 4d372a4d-ba8f-b8e4-e063-6294a90ae9d8
spl set id: 39035b99-e560-e6b6-e063-6294a90a19c6

Reported adverse events (FAERS/openFDA)#

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