Label: HAWAIIAN TROPIC MATTE EFFECT MINERAL ENRICHED SUNSCREEN SPF 30- homosalate, octisalate, octocrylene, zinc oxide lotion
- NDC Code(s): 63354-502-24
- Packager: Edgewell Personal Care Brands, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 30, 2023
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- Active Ingredients
- Purpose
- Uses
- Warnings
- May stain
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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 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, Isohexadecane, Cetyl Alcohol, Glycerin, VP/Eicosene Copolymer, PEG-100 Stearate, Glyceryl Stearate, Alcohol Denat., Silica, Phenoxyethanol, Xanthan Gum, Fragrance, Chlorphenesin, Polyhydroxystearic Acid, Disodium EDTA, Triethoxycaprylylsilane, Sea Salt, Psidium Guajava Fruit Extract, Plumeria Acutifolia Flower Extract, Passiflora Incarnata Fruit Extract, Mangifera Indica (Mango) Fruit Extract, Carica Papaya (Papaya) Fruit Extract.
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INGREDIENTS AND APPEARANCE
HAWAIIAN TROPIC MATTE EFFECT MINERAL ENRICHED SUNSCREEN SPF 30
homosalate, octisalate, octocrylene, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-502 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 5.6695 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4.5 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 6 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PLUMERIA RUBRA FLOWER (UNII: 8P7XXY759H) PAPAYA (UNII: KU94FIY6JB) SODIUM CHLORIDE (UNII: 451W47IQ8X) ISOHEXADECANE (UNII: 918X1OUF1E) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) ALCOHOL (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CETYL ALCOHOL (UNII: 936JST6JCN) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) PHENOXYETHANOL (UNII: HIE492ZZ3T) PEG-100 STEARATE (UNII: YD01N1999R) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P) CHLORPHENESIN (UNII: I670DAL4SZ) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) MANGO (UNII: I629I3NR86) GUAVA (UNII: 74O70D6VG0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-502-24 177.44 g in 1 BOTTLE; Type 0: Not a Combination Product 09/06/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/06/2019 Labeler - Edgewell Personal Care Brands, LLC (151179769)
