NDC | 63354-150-61 |
Set ID | 257591de-bc9a-4302-b915-d958f769d194 |
Category | HUMAN OTC DRUG LABEL |
Packager | Edgewell Personal Care Brands LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
-
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 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.
-
Inactive Ingredients
Petrolatum, Polyethylene, Ethylhexyl Palmitate, Trimethylsiloxyphenyl Dimethicone, Microcrystalline Wax, Isopropyl Myristate, Theobroma Cacao (Cocoa) Seed Butter, PEG-8, Caprylyl Glycol, Sodium Saccharin, Cocos Nucifera (Coconut) Oil, Mineral Oil, Aloe Barbadensis Leaf Extract, PEG-8 Dimethicone, Octyldodecanol, Retinyl Palmitate, Silica, Tocopheryl Acetate, Ascorbic Acid, Sodium Propoxyhydroxypropyl Thiosulfate Silica, Propylparaben, Butylparaben, Flavor.
- Other Information
- Questions or comments?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
BANANA BOAT
avobenzone, octocrylene, oxybenzone stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 6 g in 100 g Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POTASSIUM SODIUM SACCHARATE DIHYDATE (UNII: 6SI0K9D9KF) COCONUT OIL (UNII: Q9L0O73W7L) ALOE VERA LEAF (UNII: ZY81Z83H0X) PEG-8 DIMETHICONE (UNII: GIA7T764OD) OCTYLDODECANOL (UNII: 461N1O614Y) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ASCORBIC ACID (UNII: PQ6CK8PD0R) PROPYLPARABEN (UNII: Z8IX2SC1OH) BUTYLPARABEN (UNII: 3QPI1U3FV8) PETROLATUM (UNII: 4T6H12BN9U) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) ETHYLHEXYL PALMITATE (UNII: 2865993309) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) COCOA BUTTER (UNII: 512OYT1CRR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-150-61 4.25 g in 1 TUBE; Type 0: Not a Combination Product 08/26/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 08/26/2011 Labeler - Edgewell Personal Care Brands LLC (151179769)