ST. MORIZ SUNCARE 50 BODY SUNSCREEN- sunscreen lotion

St. Moriz Suncare 50 Body Sunscreen by

Drug Labeling and Warnings

St. Moriz Suncare 50 Body Sunscreen by is a Otc medication manufactured, distributed, or labeled by Hothouse Beauty Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredients: homosalate 10%, octocrylene 10%, octisalate 4%, avobenzone 3%

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions) decreases risk of skin cancer and early skin aging caused by the sun

Warnings

• For external use only.
• Do not use on damaged or broken skin
• When using this product [bullet] keep out of eyes. Rinse with water to remove.
• Stop use and ask a doctor if [bullet] rash or irritation develops and lasts.
• Keep out of reach of children, If product is swallowed, get medical help or contact poison control centre right away.
• To ensure compatibility, we recommend patch testing before first use. In the unlikely event of a negative reaction, discontinue use and consult your medical practitioner.

Do not use

Do not use on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Apply generously 15 minutes before sun exposure”
• Reapply [bullet] after 80 minutes of swimming or sweating [bullet] immediately after towel drying [bullet] at least every 2 hours
• Children under 6 months of age: Ask a doctor
• Sun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:  limit time in the sun, especially from 10 a.m. - 2 p.m.  wear long-sleeved shirts, pants, hats, and sunglasses

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butyloctyl Salicylate, C12-20 Alkyl Glucoside, C14-22 Alcohols, Chlorphenesin, Dimethicone/Vinyl Dimethicone Crosspolymer, Dipotassium Glycyrrhizate, Disodium Edta, Fragrance, Phenoxyethanol, Propylene Glycol, Silica, Simmondsia Chinensis (Jojoba) Seed Oil, Steareth-21, Tocopheryl Acetate, Trehalose, Triethanolamine, Water

Other Information

Protect the product in this container from excessive heat and direct sun. Store below 30 degrees celcius.

Uses

Helps prevent sunburn.

St. Moriz Suncare 50+ Body Sunscreen

NDC: 85178-2125-1

180 mL / 6.08 fl oz

Principal Display Panel and information panel primary container:

INGREDIENTS AND APPEARANCE

ST. MORIZ SUNCARE 50 BODY SUNSCREEN 
sunscreen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85178-2125
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	40 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
SILICA (UNII: ETJ7Z6XBU4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CHLORPHENESIN (UNII: I670DAL4SZ)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
JOJOBA OIL (UNII: 724GKU717M)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
TREHALOSE (UNII: B8WCK70T7I)
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
C14-22 ALCOHOLS (UNII: B1K89384RJ)
STEARETH-21 (UNII: 53J3F32P58)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85178-2125-1	180 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/20/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/20/2025

Labeler - Hothouse Beauty Inc (119438098)