FDA.reportPublic FDA data

Banana Boat - Edgewell Personal Care Brands, LLC

Manufacturer
Edgewell Personal Care Brands, LLC
Effective date
2026-05-28
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-10-02 01:04:17

Label at a glance#

ProductBanana Boat
Active ingredientAVOBENZONE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, HOMOSALATE
Label structure9 sections

Indications and uses

￭ helps prevent sunburn ￭ if used as directed with other sun protection measures ( see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

￭ 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 ￭ d o 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 ￭ children under 6 months: ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Homosalate 10.0%, Octisalate 5.0%,Octocrylene 10.0%, Oxybenzone 6.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

￭ helps prevent sunburn ￭ if used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

Flammable: Contents under pressure. Do not puncture or incinerate. 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.

Do not use

OTC - DO NOT USE SECTION

￭ on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

￭ keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

￭ rash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

￭ 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 ￭ d o 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 ￭ 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

Other information

SPL UNCLASSIFIED SECTION

￭ protect this product from excessive heat and direct sun ￭ may stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat., Isobutane, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Caprylyl Glycol, Cyclopentasiloxane, Cyclohexasiloxane, Fragrance, Polyglyceryl-3 Stearate/Isostearate/Dimer Dilinoleate Crosspolymer, Lauryl PEG-8 Dimethicone, Phenylisopropyl Dimethicone, Ascorbyl Palmitate, Methyl Dihydroabietate, Tocopheryl Acetate, Mineral Oil, Panthenol, Water, Aloe Barbadensis Leaf Extract.

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-SAFESUN, Mon-Fri

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BANANA
BOAT
100
SPORT
HIGH ENDURANCE
SUNSCREEN SPRAY
RESISTS WATER,
SWEAT & HEAT
WATER RESISTANT (80 MINUTES)
DERMATOLOGIST TESTED
BROAD SPECTRUM UVA/UVB SPF 100
NET WT. 6. OZ. (170 g)

FULL LABELFULL LABEL

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63354-20663354-206-34

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OXYBENZONE95OOS7VE0YACTIB
HOMOSALATEV06SV4M95SACTIB
ALCOHOL3K9958V90MIACT
ISOBUTANEBXR49TP611IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ASCORBYL PALMITATEQN83US2B0NIACT
METHYL DIHYDROABIETATE7666FJ0J9FIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
MINERAL OILT5L8T28FGPIACT
PANTHENOLWV9CM0O67ZIACT
CYCLOMETHICONE 6XHK3U310BAIACT
LAURYL PEG-8 DIMETHICONE (300 CPS)ELL2U7K8T8IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62023-11-06full-release2026-05-31 23:59:17

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
098345af-981a-77dd-e063-6294a90aa11e46feef09-69ae-41b4-e054-00144ff8d46c2023-11-06WarningsExact identifier
spl set id: 46feef09-69ae-41b4-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.