ST MORIZ SUNCARE FACE SUNSCREEN SPF30- suncare face sunscreen spf30 lotion

ST MORIZ SUNCARE FACE SUNSCREEN SPF30 by

Drug Labeling and Warnings

ST MORIZ SUNCARE FACE SUNSCREEN SPF30 by is a Otc medication manufactured, distributed, or labeled by Aopline Biotechnology (Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

OCTISALATE
TITANIUM DIOXIDE
OCTOCRYLENE

PURPOSE

Uses: Helps prevent sunburn.

WARNINGS

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 .

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Immediately after towel drying.
At least every 2 hours.

INDICATIONS & USAGE

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ST MORIZ SUNCARE FACE SUNSCREEN SPF30 
suncare face sunscreen spf30 lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87283-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	9 g  in 180 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	5.4 g  in 180 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5.4 g  in 180 mL

Inactive Ingredients
Ingredient Name	Strength
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
CYCLOHEXASILOXANE (UNII: XHK3U310BA)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
XANTHAN GUM (UNII: TTV12P4NEE)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
ALCOHOL (UNII: 3K9958V90M)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 60 (UNII: CAL22UVI4M)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
STEARIC ACID (UNII: 4ELV7Z65AP)
CHLORPHENESIN (UNII: I670DAL4SZ)
BEHENYL ALCOHOL (UNII: 9G1OE216XY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87283-008-01	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/09/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/09/2026

Labeler - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)

Registrant - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)