Label: HAWAIIN TROPIC SILK HYDRATION DRY BROAD SPECTRUM SPF 30- avobenzone,homosalate,octisalate,octocrylene oil
- NDC Code(s): 63354-632-13
- Packager: Edgewell Personal Care Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 24, 2023
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- Active ingredients
- Purpose
- Uses
- Warnings
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Directions
• apply liberally 15 minutes before sun exposure • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • 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 longsleeved shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor
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Inactive Ingredients
Alcohol Denat., Isododecane, Diisopropyl Adipate, Mineral Oil, Phenylisopropyl Dimethicone, Polyglyceryl-3 Stearate/Isostearate/Dimer Dilinoleate Crosspolymer, Lauryl PEG-8 Dimethicone, Caprylyl Glycol, Methyl Dihydroabietate, Fragrance, Tocopheryl Acetate, Ascorbyl Palmitate, Cocos Nucifera (Coconut) Oil, Vitis Vinifera (Grape) Seed Oil, Olea Europaea (Olive) Fruit Oil, Argania Spinosa Kernel Oil, Water, Panthenol, Carica Papaya (Papaya) Fruit Extract, Mangifera Indica (Mango) Fruit Extract, Passiflora Incarnata Fruit Extract, Plumeria Acutifolia Flower Extract, Psidium Guajava Fruit Extract, Aloe Barbadensis Leaf Extract
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INGREDIENTS AND APPEARANCE
HAWAIIN TROPIC SILK HYDRATION DRY BROAD SPECTRUM SPF 30
avobenzone,homosalate,octisalate,octocrylene oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-632 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 6 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 6 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) GRAPE SEED OIL (UNII: 930MLC8XGG) WATER (UNII: 059QF0KO0R) LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) ASCORBYL PALMITATE (UNII: QN83US2B0N) COCONUT OIL (UNII: Q9L0O73W7L) OLIVE OIL (UNII: 6UYK2W1W1E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ARGAN OIL (UNII: 4V59G5UW9X) PANTHENOL (UNII: WV9CM0O67Z) MANGO (UNII: I629I3NR86) PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P) GUAVA (UNII: 74O70D6VG0) ALCOHOL (UNII: 3K9958V90M) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) ISODODECANE (UNII: A8289P68Y2) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PAPAYA (UNII: KU94FIY6JB) PLUMERIA RUBRA FLOWER (UNII: 8P7XXY759H) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-632-13 142 g in 1 BOTTLE; Type 0: Not a Combination Product 09/25/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/25/2020 Labeler - Edgewell Personal Care Brands LLC (151179769)
