BANANA BOAT

Manufacturer
Edgewell Personal Care Brands LLC
Effective date
2018-12-05
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-02 00:44:35

Label at a glance#

ProductBANANA BOAT
Active ingredientAVOBENZONE, OCTOCRYLENE, OXYBENZONE
Label structure9 sections

Dosage and administration

apply generously and evenly to all areas 15 minutes before sun exposure spray on hands to apply to face use in well-ventilated area reapply at frequent intervals and after swimming or towel drying ask a doctor before use on children under six months of age

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 1%, Octocrylene 7.7%, Oxybenzone 3%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

helps prevent sunburn

Warnings

WARNINGS SECTION

  • For external use only
  • Do not spray directly into flame
  • Flammable: do not use near hat, flame, or while smoking

When using this product

OTC - WHEN USING SECTION

avoid spraying in eyes. If contact occurs, rinse throughly with water.

do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120F

stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply generously and evenly to all areas 15 minutes before sun exposure
  • spray on hands to apply to face
  • use in well-ventilated area
  • reapply at frequent intervals and after swimming or towel drying
  • ask a doctor before use on children under six months of age

Other Information

SPL UNCLASSIFIED SECTION

Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.

May stain some fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat., Acrylates/Octylacrylamide Copolymer, Caprylyl Glycol, PEG-8 Dimethicone, Aloe Barbadensis Leaf Extract, Mineral Oil, Octyldodecanol, Retinyl Palmitate, Silica, Tocopheryl Acetate, Ascorbic Acid, Sodium PropoxyhydroxypropylThiosulfate Silica, Fragrance.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-800 SafeSun, Mon-Fri

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BANANA

BOAT

Quik Dri

SPORT

body & scalp

Advanced UVA/UVB Sunscreen

SPF 30

UVB

High UVA

long lasting protection

sun tested, sun proven

non greasy, Oil free

Won't run into eyes

Very water/sweat resistant

93002542930025429300254393002543

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX5
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WM5
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y5
AVOBENZONEACTIVE MOIETYG63QQF2NOX5
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM5
OXYBENZONEACTIVE MOIETY95OOS7VE0Y5

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63354-93063354-930-34, 63354-930-36, 63354-930-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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
0afb7879-94ab-37df-e063-6294a90a42569dea8499-635f-4c01-8d05-5cef4bf3e0622023-11-25WarningsExact identifier
spl set id: 9dea8499-635f-4c01-8d05-5cef4bf3e062

Reported adverse events (FAERS/openFDA)#

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