Label: BANANA BOAT- avobenzone octocrylene oxybenzone lotion
- NDC Code(s): 63354-911-53
- Packager: Edgewell Personal Care Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 9, 2023
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- Active Ingredients
- Purpose
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- 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, regulrly 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-sleeve shirts, pants, hats, and sunglasses • children under 6 months: Ask a doctor
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Inactive ingredients
Water, Hydrogenated Polyisobutene, Lauryl PEG-8 Dimethicone, Butyloctyl Salicylate, Ethylhexyl Palmitate, Hydrated Silica, Cyclopentasiloxane, Cyclohexasiloxane, Sodium Chloride, Benzyl Alcohol, Beeswax, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Methylparaben, Microcrystalline Wax, Polyethylene, Caprylyl Glycol, Propylparaben, Disodium EDTA, Stearoxy Dimethicone, Methyl Dihydroabietate, Phenylisopropyl Dimethicone, Polyglyceryl-3 Stearate/Isostearate/Dimer Dilinoleate Crosspolymer, Sodium Ascorbyl Phosphate, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice.
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INGREDIENTS AND APPEARANCE
BANANA BOAT
avobenzone octocrylene oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-911 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 8 g in 100 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 3.5 g in 100 g Inactive Ingredients Ingredient Name Strength CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) BENZYL ALCOHOL (UNII: LKG8494WBH) METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O) ALOE VERA LEAF (UNII: ZY81Z83H0X) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ETHYLHEXYL PALMITATE (UNII: 2865993309) HYDRATED SILICA (UNII: Y6O7T4G8P9) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) SODIUM CHLORIDE (UNII: 451W47IQ8X) YELLOW WAX (UNII: 2ZA36H0S2V) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-911-53 118 g in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/19/2015 Labeler - Edgewell Personal Care Brands LLC (151179769)