Label: BANANA BOAT PROTECTION PLUS VITAMINS SUNSCREEN UVA/UVB BROAD SPECTRUM SPF 50- avobenzone,homosalate,octisalate,octocrylene lotion
- NDC Code(s): 63354-571-23
- 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
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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 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, Diisopropyl Adipate, Niacinamide, Cetearyl Alcohol, Phenoxyethanol, Carbomer, Benzyl Alcohol, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Ascorbyl Glucoside, Glycerin, Chlorphenesin, Dicetyl Phosphate, Ceteth-10 Phosphate, Coco Glucoside,
Sodium Hydroxide, Propylene Glycol, Cocos Nucifera (Coconut) Oil, Xanthan Gum, Disodium EDTA, Camellia Sinensis Leaf Extract, Fragrance, Mica, Tocopheryl Acetate, Titanium Dioxide, Iron Oxides. - Other Information
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INGREDIENTS AND APPEARANCE
BANANA BOAT PROTECTION PLUS VITAMINS SUNSCREEN UVA/UVB BROAD SPECTRUM SPF 50
avobenzone,homosalate,octisalate,octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-571 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 HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 5 g in 100 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) NIACINAMIDE (UNII: 25X51I8RD4) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) GLYCERIN (UNII: PDC6A3C0OX) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) PHENOXYETHANOL (UNII: HIE492ZZ3T) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) WATER (UNII: 059QF0KO0R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MICA (UNII: V8A1AW0880) BENZYL ALCOHOL (UNII: LKG8494WBH) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CHLORPHENESIN (UNII: I670DAL4SZ) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) XANTHAN GUM (UNII: TTV12P4NEE) COCONUT OIL (UNII: Q9L0O73W7L) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCO GLUCOSIDE (UNII: ICS790225B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-571-23 133 g in 1 TUBE; Type 0: Not a Combination Product 10/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/01/2022 Labeler - Edgewell Personal Care Brands LLC (151179769)
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