FDA.reportPublic FDA data

FACE SPF 47 SETTING

Manufacturer
Aopline Biotechnology (Guangzhou) Co., Ltd.
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:32:01

Label at a glance#

ProductFACE SPF 47 SETTING
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTISALATE, HOMOSALATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Homosalate 8.0%

Octisalate 5.0%

Octocrylene 3.0%

Avobenzone 3.0%

OTC - PURPOSE SECTION

Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

For External Use Only.

Do not use on damaged or broken skin.

Keep out of reach of children.

Keep out of eyes. Rinse with water to remove.

Stop use and ask a physician if rash occurs.

Keep out of reach of children . If product is swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

•Apply to face 15 minutes before sun exposure.

Reapply every 2 hours.

INACTIVE INGREDIENT SECTION

Vitamin E, Vitamin C, Hyaluronic Acid, Niacinamide, Peppermint Extract, Eucalyptus Extract, Sunflower Seed Oil, Tea Tree Extract, Alcohol, Cyclohexasiloxane, Cyclopentasiloxane, Ethylhexyl Palmitate

INDICATIONS & USAGE SECTION

Helps prevent sunburn. If used as directed with other sun protection measures, decrease the risk of skin cancer and early skin aging caused by sun.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87283-001-01FACE SPF 47 SETTING50 mL in 1 BOTTLESPRAY501

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87283-00187283-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALCOHOL3K9958V90MIACT
HYALURONIC ACIDS270N0TRQYIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
OCTOCRYLENE5A68WGF6WMACTIB
SUNFLOWER OIL3W1JG795YIIACT
CYCLOMETHICONE 6XHK3U310BAIACT
NIACINAMIDE25X51I8RD4IACT
PEPPERMINTV95R5KMY2BIACT
CYCLOMETHICONE 50THT5PCI0RIACT
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
HOMOSALATEV06SV4M95SACTIB
ETHYLHEXYL PALMITATE2865993309IACT
ASCORBIC ACIDPQ6CK8PD0RIACT

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
FACE SPF 47 SETTINGFACE SPF 47 SETTING SPRAYAopline Biotechnology (Guangzhou) Co., Ltd.47db9a54-c02f-d2ea-e063-6394a90ab9732026-01-08WarningsExact identifier
ndc (package): 87283-001-01
ndc (product): 87283-001
ndc11 (package): 87283000101
spl id: 47db9a54-c030-d2ea-e063-6394a90ab973
spl set id: 47db9a54-c02f-d2ea-e063-6394a90ab973

Reported adverse events (FAERS/openFDA)#

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