Label: HAWAIIAN TROPIC INVISIBLE SUNSCREEN SHEER TOUCH SPF 30- avobenzone,homosalate,octisalate,octocrylene liquid
- NDC Code(s): 63354-195-22
- 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 two 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 long-sleeved shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor
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Inactive Ingredients
Water, Silica, Propylene Glycol, Cetyl Dimethicone, Phenoxyethanol, Mica, Sodium Polyacrylate, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Caprylyl Glycol, Fragrance, Chlorphenesin, Glycerin, Disodium EDTA, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate, Hibiscus Sabdariffa Flower Extract, Carica Papaya (Papaya) Fruit Extract, Mangifera Indica (Mango) Fruit Extract, Passiflora Incarnata
Fruit Extract, Plumeria Acutifolia Flower Extract, Psidium Guajava Fruit Extract, Titanium Dioxide.
- Other Information
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INGREDIENTS AND APPEARANCE
HAWAIIAN TROPIC INVISIBLE SUNSCREEN SHEER TOUCH SPF 30
avobenzone,homosalate,octisalate,octocrylene liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-195 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 6 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4.5 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.7 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MICA (UNII: V8A1AW0880) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) CHLORPHENESIN (UNII: I670DAL4SZ) GLYCERIN (UNII: PDC6A3C0OX) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ALOE VERA LEAF (UNII: ZY81Z83H0X) HIBISCUS SABDARIFFA FLOWER (UNII: 45TGG6IU6M) PAPAYA (UNII: KU94FIY6JB) PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P) GUAVA (UNII: 74O70D6VG0) PLUMERIA RUBRA FLOWER (UNII: 8P7XXY759H) PHENOXYETHANOL (UNII: HIE492ZZ3T) ACRYLIC ACID (UNII: J94PBK7X8S) MANGO (UNII: I629I3NR86) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-195-22 97 g in 1 TUBE; Type 0: Not a Combination Product 10/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/01/2022 Labeler - Edgewell Personal Care Brands LLC (151179769)
