Label: BANANA BOAT- avobenzone, homosalate, octisalate, octocrylene aerosol, spray
- NDC Code(s): 63354-788-31, 63354-788-34, 63354-788-36, 63354-788-37
- Packager: Edgewell Personal Care Brands, LLC
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 22, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- when using this product
- Stop use and ask a dcotor
- Keep out of reach of children
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flammable
Contents under pressure. Do not puncture or incinerate container. Do not expose to heat or store at temperatures above 120°F. Do not use in the presence of a flame or spark. Keep away from sources of ignition - No smoking. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
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Directions
- Shake well.
- Hold container 4 to 6 inches from the skin to apply
- Spray liberally and spread evenly by hand 15 minutes before sun exposure
- Do not spray directly into face. Spray on hands and then apply to face.
- Do not apply in windy conditions •Use in a well-ventilated area •Reapply: •after 80 minutes of swimming or sweating •immediately after towel drying •at least every 2 hours
- Children under 6 months: Ask a doctor
- 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.
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Inactive Ingredients
Water, Isobutane, Isohexadecane, Ethylhexyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone,Lauryl PEG-8 Dimethicone, Dibutyl Adipate, Ethylhexyl Methoxycrylene, Sodium Chloride,PEG-8, Phenoxyethanol, Caprylyl Glycol, Glycerin, Sodium Citrate, Methylparaben,Butylparaben, Ethylparaben, Isobutylparaben, Propylparaben, Methyl Dihydroabietate,Phenylisopropyl Dimethicone, Polyglyceryl-3 Stearate/Isostearate/Dimer Dilinoleate Crosspolymer, PEG-8 Dimethicone, Aloe Barbadensis Leaf Juice, Octyldodecanol, Retinyl Palmitate, Silica, Tocopheryl Acetate, Ascorbic Acid, Sodium Propoxyhydroxypropyl Thiosulfate Silica.
- Other Information
- Questions or Comments?
- Front Label
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INGREDIENTS AND APPEARANCE
BANANA BOAT
avobenzone, homosalate, octisalate, octocrylene aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-788 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 6 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ISOBUTANE (UNII: BXR49TP611) ISOHEXADECANE (UNII: 918X1OUF1E) DIBUTYL ADIPATE (UNII: F4K100DXP3) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CITRATE (UNII: 1Q73Q2JULR) METHYLPARABEN (UNII: A2I8C7HI9T) BUTYLPARABEN (UNII: 3QPI1U3FV8) ETHYLPARABEN (UNII: 14255EXE39) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) PEG-8 DIMETHICONE (UNII: GIA7T764OD) OCTYLDODECANOL (UNII: 461N1O614Y) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) ASCORBIC ACID (UNII: PQ6CK8PD0R) SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332) ETHYL BENZOATE (UNII: J115BRJ15H) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-788-31 51 g in 1 CAN; Type 0: Not a Combination Product 01/02/2017 2 NDC:63354-788-34 170 g in 1 CAN; Type 0: Not a Combination Product 01/02/2017 3 NDC:63354-788-36 227 g in 1 CAN; Type 0: Not a Combination Product 01/02/2017 4 NDC:63354-788-37 269 g in 1 CAN; Type 0: Not a Combination Product 11/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/02/2017 Labeler - Edgewell Personal Care Brands, LLC (151179769)