FDA.reportPublic FDA data

ST MORIZ SUNCARE FACE SUNSCREEN SPF30

Manufacturer
Aopline Biotechnology (Guangzhou) Co., Ltd.
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:52:27

Label at a glance#

ProductST MORIZ SUNCARE FACE SUNSCREEN SPF30
Active ingredientOCTISALATE, TITANIUM DIOXIDE, OCTOCRYLENE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OCTISALATE
TITANIUM DIOXIDE
OCTOCRYLENE

OTC - PURPOSE SECTION

Uses: Helps prevent sunburn.

WARNINGS SECTION

For external use only .
Do not use on broken or damaged skin .
Stop use and ask a doctor if rash occurs
When using this product keep out of eyes . Rinse with water to remove .
Keep out of reach of children . If product is swallowed , get medical help or contact a
Poison Control Center right away .

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Immediately after towel drying.
At least every 2 hours.

INDICATIONS & USAGE SECTION

Directions : Apply liberally 15 minutes before sun or water exposure. Works best on
moisturized skin.
Reapply:
After 80 minutes of swimming or sweating.
Immediately after towel drying.
At least every 2 hours.
Children under 6 months: Ask a doctor.

INACTIVE INGREDIENT SECTION

CYCLOHEXASILOXANE
WATER
CYCLOPENTASILOXANE
GLYCERIN
PROPYLENE GLYCOL
ALCOHOL
CETYL ETHYLHEXANOATE
ALUMINUM HYDROXIDE
STEARIC ACID
DIPROPYLENE GLYCOL
C12-15 ALKYL BENZOATE
ARACHIDYL ALCOHOL
BEHENYL ALCOHOL
ARACHIDYL GLUCOSIDE
PHENOXYETHANOL
1,2-HEXANEDIOL
CHLORPHENESIN
POLYSORBATE 60
ALLANTOIN
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
TRIETHANOLAMINE
XANTHAN GUM
DISODIUM EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87283-008-01ST MORIZ SUNCARE FACE SUNSCREEN SPF30180 mL in 1 BOTTLELOTION1801

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87283-00887283-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
CETYL ETHYLHEXANOATE134647WMX4IACT
CYCLOHEXASILOXANEXHK3U310BAIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
XANTHAN GUMTTV12P4NEEIACT
DIPROPYLENE GLYCOLE107L85C40IACT
ALCOHOL3K9958V90MIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
TRIETHANOLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
ALLANTOIN344S277G0ZIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 60CAL22UVI4MIACT
OCTISALATE4X49Y0596WACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
EDETATE DISODIUM7FLD91C86KIACT
STEARIC ACID4ELV7Z65APIACT
CHLORPHENESINI670DAL4SZIACT
OCTOCRYLENE5A68WGF6WMACTIB
BEHENYL ALCOHOL9G1OE216XYIACT

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
ST MORIZ SUNCARE FACE SUNSCREEN SPF30SUNCARE FACE SUNSCREEN SPF30Aopline Biotechnology (Guangzhou) Co., Ltd.47f26af6-4d02-3506-e063-6294a90a0fe62026-01-09WarningsExact identifier
ndc (package): 87283-008-01
ndc (product): 87283-008
ndc11 (package): 87283000801
spl id: 47f26af6-4d03-3506-e063-6294a90a0fe6
spl set id: 47f26af6-4d02-3506-e063-6294a90a0fe6

Reported adverse events (FAERS/openFDA)#

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