Label: ST MORIZ SUNCARE BODY SUNSCREEN SPF30- suncare body sunscreen spf30 lotion
- NDC Code(s): 82723-013-01
- Packager: Aopline Health Industry Technology (Guangzhou) Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 26, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
-
Inactive ingredient
PROPYLENE GLYCOL
WATER
BUTYLOCTYL SALICYLATE
GLYCERETH-20
ISOSTEARETH-20
ISOCETETH-20
LAURIC/MYRISTIC/PALMITIC/STEARIC GLYCERIDES
GLYCERYL STEARATE
ALUMINUM STARCH OCTENYLSUCCINATE
PHENOXYETHANOL
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
TRIETHANOLAMINE
CHLORPHENESIN
FRAGRANCE
DISODIUM EDTA
XANTHAN GUM - PURPOSE
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Warning
For extemal use onl,.
Do not use on damaged or broken skn,
When using this product keep out of cyes, Rinse withwater to remowe,
Siop use and ask a doctor if rash cccurs.Keep out of reach of children, lf product is swalkawed, getmedical help or contact a Potson Conirol Centre right away.Wlay stain some fabrics.
- stop to use
- Do not use
- When
- KEEP OUT OF REACH OF CHILDREN
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Indication
Directions: Apply liberaly 15 minues before sunexposure,
Reapply: After 80 minutes of swimming or sseating,
lmmedabely after towel drying.
At least every 2 hours,
Children under 6 months: Ask a Doctor
Sun Protection Measures: spendng time in the suni ncreases your risk of skin caner and early skin aging.
To decrease this risk, regulary use a sunsereen with a broad spectrum spf value of 15 or higher and other sun protection measure including, lmit time in the sun,especially from 10a,m. to 2p.m, Wear long-sleeved shirtspanis, hats, and sunglasses,
- DOSAGE & ADMINISTRATION
- labeling
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INGREDIENTS AND APPEARANCE
ST MORIZ SUNCARE BODY SUNSCREEN SPF30
suncare body sunscreen spf30 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82723-013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 14.4 mg in 180 mL GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 10.9 mg in 180 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 9 mg in 180 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 5.4 mg in 180 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 7.2 mg in 180 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERYL STEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) WATER (UNII: 059QF0KO0R) GLYCERETH-20 (UNII: GJ57297I4F) TRIETHANOLAMINE (UNII: 9O3K93S3TK) CHLORPHENESIN (UNII: I670DAL4SZ) XANTHAN GUM (UNII: TTV12P4NEE) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ISOSTEARETH-20 (UNII: 78H2SJ8X8M) ISOCETETH-20 (UNII: O020065R7Z) LAURIC ACID (UNII: 1160N9NU9U) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82723-013-01 180 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/01/2025 Labeler - Aopline Health Industry Technology (Guangzhou) Co., Ltd. (715076108)

