ST MORIZ SUNCARE SPF 50 SUNSCREEN BODY (homosalate octocrylene ethylhexyl salicylate (octisalate) butyl methoxydibenzoylmethane- avobenzone spray

St Moriz Suncare SPF 50 Sunscreen Body by

Drug Labeling and Warnings

St Moriz Suncare SPF 50 Sunscreen Body by is a Otc medication manufactured, distributed, or labeled by Aopline Health Industry Technology (Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Homosalate
Octocrylene
Ethylhexyl Salicylate
(Octisalate)
Butyl Methoxydibenzoylmethane
(Avobenzone)

PURPOSE

Helps prevent sunburn. lf used as directedwith other sun protection measures (see Directions).decreases the risk of skin cancer and early agingcaused by the sun.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. if product isswallowed, get medical help or contact a PoisonControl Centre right away

WARNINGS

WarningsFlammable. Do nat use near heat, flame, or whilesmoking. Contents under pressure. Do not puncture orincinerate, Do not store at temperature above 120 °F
For external use only.

INACTIVE INGREDIENT

Inactive Ingredients: Alcohol Denat. C12-15Alkyl Benzoate, Acrylates/ 0ctacrylamide Copolymer,PPG-5-Ceteth-20, Aloe Barbadensis Leaf ExtractFragrance, Tocopherol.

INDICATIONS & USAGE

Sun Protection Measures: Spendingtime in the sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use asunscreen with a broad spectrum spf value of 15 orhigher and other sun protection measure including:limit time in the sun, especially from 10a.m. to 2p.m.Wear long-sleeved shirts, pants, hats, and sunglasses

DOSAGE & ADMINISTRATION

Apply liberally 15 minutes before sunexposure, Reapply: After 80 minutes of swimmingor sweating." immediately after towel dryingAt least every 2 hours. Children under 6 months.Ask a doctor

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ST MORIZ SUNCARE SPF 50 SUNSCREEN BODY 
homosalate octocrylene ethylhexyl salicylate (octisalate) butyl methoxydibenzoylmethane (avobenzone) spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82723-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ETHYLHEXYL SALICYLATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	ETHYLHEXYL SALICYLATE	5 g  in 100 mL
BUTYL METHOXYDIBENZOYLMETHANE (UNII: G63QQF2NOX) (BUTYL METHOXYDIBENZOYLMETHANE - UNII:G63QQF2NOX)	BUTYL METHOXYDIBENZOYLMETHANE	3 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	7 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
ALCOHOL (UNII: 3K9958V90M)
FRAGRANCE 13576 (UNII: 5EM498GW35)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
TOCOPHEROL (UNII: R0ZB2556P8)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82723-020-01	162 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/02/2025

Labeler - Aopline Health Industry Technology (Guangzhou) Co., Ltd. (715076108)

Registrant - Aopline Health Industry Technology (Guangzhou) Co., Ltd. (715076108)