NDC | 63354-110-21, 63354-110-22 |
Set ID | c118d568-58ca-42f4-a34d-2fc0c17b85e0 |
Category | HUMAN OTC DRUG LABEL |
Packager | Edgewell Personal Care Brands LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children
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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
•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, Butyloctyl Salicylate, Ethylhexyl Benzoate, Silica, Hydrogenated Dimer Dilinoleyl/Dimethylcarbonate Copolymer, Stearyl Alcohol, Glycerin, Caprylyl Glycol, Phenoxyethanol,Triethanolamine, Cetyl Alcohol, Carbomer, Methylparaben, Glyceryl Stearate, Behenyl Alcohol, Xanthan Gum, Sodium Lauroyl Sarcosinate, Disodium EDTA, Propylparaben, BHT,Disodium Ethylene Dicocamide PEG-15 Disulfate, Glyceryl Stearate Citrate, Glucosamine HCl,Cetearyl Alcohol, Sodium Lauroyl Lactylate, Pisum Sativum (Pea) Extract, Retinyl Palmitate,Tocopheryl Acetate, Bambusa Vulgaris Leaf/Stem Extract, Lecithin, Aloe Barbadensis Leaf Juice.
- Other information
- Questions or comments?
- PDP
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INGREDIENTS AND APPEARANCE
BANANA BOAT
avobenzone, octocrylene, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-110 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 OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 4 g in 100 g Inactive Ingredients Ingredient Name Strength 2-ETHYLHEXYL BENZOATE (UNII: R63ZWW1A13) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TROLAMINE (UNII: 9O3K93S3TK) CETYL ALCOHOL (UNII: 936JST6JCN) METHYLPARABEN (UNII: A2I8C7HI9T) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) EDETATE DISODIUM (UNII: 7FLD91C86K) PROPYLPARABEN (UNII: Z8IX2SC1OH) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) BAMBUSA VULGARIS LEAF (UNII: EMY54R518C) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) XANTHAN GUM (UNII: TTV12P4NEE) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) PISUM SATIVUM WHOLE (UNII: J21YE3W98E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63354-110-21 29 g in 1 TUBE; Type 0: Not a Combination Product 12/01/2011 12/31/2017 2 NDC:63354-110-22 88 g in 1 TUBE; Type 0: Not a Combination Product 12/01/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 12/01/2011 Labeler - Edgewell Personal Care Brands LLC (151179769)