Label: BANANA BOAT KIDS MINERAL VANISHING GREEN FOAM SPF 50 AMAZING APPLE- titanium dioxide, zinc oxide aerosol, foam
- NDC Code(s): 23667-050-04
- Packager: Formulated Solutions, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 30, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
- Shake well
- Dispense in upright position for optimal results
- 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 then apply to face
- Do not apply in windy conditions
- Use in well-ventilated area
- Reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours
- 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 Sun Protection Measures.
- Children under 6 months: Ask a doctor.
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Inactive Ingredients
Water, Isobutane, Caprylic/Capric Triglyceride, Isohexadecane, Butyloctyl Salicylate, Cetyl PEG/PPG-10/1 Dimethicone, Lauryl PEG-8 Dimethicone, VP/Eicosene Copolymer, Sodium Chloride, Ethylhexyl Methoxycrylene, Dimethicone, Polyhydroxystearic Acid, Phenoxyethanol, PEG-8, Caprylyl Glycol, Alumina, Fragrance, Glycerin, Sodium Citrate, Tocopheryl Acetate, Yellow 11, Green 6.
- Other information
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INGREDIENTS AND APPEARANCE
BANANA BOAT KIDS MINERAL VANISHING GREEN FOAM SPF 50 AMAZING APPLE
titanium dioxide, zinc oxide aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23667-050 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 49 mg in 1 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 71 mg in 1 g Inactive Ingredients Ingredient Name Strength TRICAPRIN (UNII: O1PB8EU98M) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) WATER (UNII: 059QF0KO0R) ISOBUTANE (UNII: BXR49TP611) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ISOHEXADECANE (UNII: 918X1OUF1E) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) SODIUM CHLORIDE (UNII: 451W47IQ8X) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) DIMETHICONE (UNII: 92RU3N3Y1O) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ALUMINUM OXIDE (UNII: LMI26O6933) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CITRATE (UNII: 1Q73Q2JULR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) D&C YELLOW NO. 11 (UNII: 44F3HYL954) D&C GREEN NO. 6 (UNII: 4QP5U84YF7) PEG-8 DIMETHICONE (UNII: GIA7T764OD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23667-050-04 113 g in 1 CAN; Type 0: Not a Combination Product 04/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/01/2021 Labeler - Formulated Solutions, LLC (143266687)
