FDA.reportPublic FDA data

SUNSCREEN SETTING SPRITZ, SPF 45

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 01:32:02

Label at a glance#

ProductSUNSCREEN SETTING SPRITZ, SPF 45
Active ingredientOCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE G63QQF2NOX 2.9%
OCTISALATE 4X49Y0596W 4.9%
OCTOCRYLENE 5A68WGF6WM 9.5%

OTC - PURPOSE SECTION

Sunscreen+ Setting Spritz

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.lf swallowed, get medical help or contacta Poison Control Center right away

INDICATIONS & USAGE SECTION

Sun Protection Measures, Spending time in the sun increases your riskof skan cancer and early skin aging. lo decrease this risk, regularly use asunscreen with a Broad Spectrum SPF value of 15 or higher and other sunprotection measures including, limit time in sun, especiallv from 10 a.m.-2p.m, and wear long-sleeved shirts, pants, hats, and sunalasses. Chitdrenunder 6 months of age: ask a doctor.

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure. Reaooly. at least every 2 hours or after 80 minutes ofswimming or sweating.

INACTIVE INGREDIENT SECTION

WATER
BHT
ALCOHOL
PEG-400
PROPYLENE GLYCOL LAURATE

WARNINGS SECTION

Warnings
For external use only Do not use on damaged or broken skin.
When using this product: keep out of eyes, Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children.lf swallowed, get medical help or contacta Poison Control Center right away
Flammable. Do not spray near heat sparks, sources of ignition, or flames

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87283-005-01SUNSCREEN SETTING SPRITZ, SPF 4560 mL in 1 BOTTLESPRAY601

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87283-00587283-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL MONOLAURATE668Z5835Z3IACT
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
AVOBENZONEG63QQF2NOXACTIB
BHT1P9D0Z171KIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT

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
SUNSCREEN SETTING SPRITZ, SPF 45SUNSCREEN SETTING SPRAYAopline Biotechnology (Guangzhou) Co., Ltd.47ddf752-cae2-313f-e063-6294a90a7e3a2026-01-08WarningsExact identifier
ndc (package): 87283-005-01
ndc (product): 87283-005
ndc11 (package): 87283000501
spl id: 47ddf752-cae3-313f-e063-6294a90a7e3a
spl set id: 47ddf752-cae2-313f-e063-6294a90a7e3a

Reported adverse events (FAERS/openFDA)#

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