Label: BANANA BOAT SPORT ULTRA SUNSCREEN BROAD SPECTRUM SPF 65- avobenzone,homosalate,octisalate,octocrylene lotion
- NDC Code(s): 63354-271-16
- Packager: Edgewell Personal Care Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2023
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- Active Ingredients
- Purpose
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Directions
• shake well •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 long-sleeved shirts, pants, hats, and
sunglasses • children under 6 months: Ask a doctor -
Inactive Ingredients
Water, PEG-100 Stearate, Glyceryl Stearate, Ethylhexyl Methoxycrylene, Cetyl Alcohol, Cetyl Dimethicone, Propylene Glycol, Phenoxyethanol, Caprylyl Glycol, VP/Eicosene Copolymer, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Sodium Polyacrylate, Chlorphenesin, Behenyl Alcohol, Xanthan Gum, Disodium EDTA, Fragrance, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice.
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INGREDIENTS AND APPEARANCE
BANANA BOAT SPORT ULTRA SUNSCREEN BROAD SPECTRUM SPF 65
avobenzone,homosalate,octisalate,octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-271 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.7 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 6.5 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 13.5 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERYL 1-STEARATE (UNII: 258491E1RZ) CETYL ALCOHOL (UNII: 936JST6JCN) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHLORPHENESIN (UNII: I670DAL4SZ) PEG-100 STEARATE (UNII: YD01N1999R) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DOCOSANOL (UNII: 9G1OE216XY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-271-16 236 g in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/15/2021 Labeler - Edgewell Personal Care Brands LLC (151179769)