FDA.reportPublic FDA data

Banana Boat Sport Body and Scalp SPF 30

Manufacturer
Accra-Pac, Inc.
Effective date
2010-03-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:01

Label at a glance#

ProductBanana Boat Sport Body and Scalp SPF 30
Active ingredientHOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, AVOBENZONE
Label structure7 sections

Dosage and administration

Apply generously and evenly (equivalent to 3 tablespoons) to all areas before sun exposure. Spray on hands to apply to face. Do not spray on face. Reapply at frequent intervals, after swimming and towel drying. For external use only. Avoid contact with eyes and fabrics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Homosalate 0.0878mL / 1mL

Octinoxate 0.05mL / 1mL

Octisalate 0.05mL / 1mL

Octocrylene 0.025mL / 1mL

Oxybenzone 0.05mL / 1mL

Avobenzone 0.03mL / 1mL

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Apply generously and evenly (equivalent to 3 tablespoons) to all areas before sun exposure. Spray on hands to apply to face. Do not spray on face. Reapply at frequent intervals, after swimming and towel drying. For external use only. Avoid contact with eyes and fabrics.

USAGE ADVICE:

OTC - WHEN USING SECTION

Do not stay too long in the sun even while using a sun protection product. Keep babies and young children out of direct sunlight. Use clothing and sun protection products with a very high SPF (higher than 25) for babies and young children.

CAUTION:

PRECAUTIONS SECTION

Over-exposure to the sun is a serious health threat. Reducing applied quantity will lower the level of protection significantly.

WARNING:

WARNINGS SECTION

FLAMMABLE. DO NOT SPRAY ON NAKED FLAME OR ANY INCANDESCENT MATERIAL. KEEP AWAY FROM FLAMES, SPARKS OR SOURCES OF IGNITION.

KEEP OUT OF REACH OF CHILDREN.

INGREDIENTS:

INACTIVE INGREDIENT SECTION

Alcohol Denat., Homosalate, C12-15 Alkyl Benzoate, Ethylhexyl Salicylate, Ethylhexyl Methoxycinnamate, Benzophenone-3, Butyl Methoxydibenzoylmethane, Octocrylene, Acrylates/Octylacrylamide Copolymer, Caprylyl Glycol, Aloe barbadensis, Retinyl Palmitate, Tocopherol, Dimethyl Capramide, Parfum, Alpha-isomethyl Ionone, Amyl Cinnamal, Benzyl Benzoate, Butylphenyl Methylpropional, Geraniol, Hexyl Cinnamal, Hydroxyisohexyl 3-Cyclohexene Carboxaldehyde, Limonene, Linalool.
Contains Oxybenzone.

MADE IN U.S.A
DISTRIBUTED BY:
ENERGIZER GROUP LTD
SWORD HOUSE, HP13 6DG
HIGH WYCOMBE, UK
www.bananaboat.co.uk

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BANANA
BOAT®
QUICK DRY
SPORT
Body & Scalp
Rub-Free Sun Protection Spray
SPF 30 UVA
AvoTriplexTM
High Protection
Sun-Tested, Sun-ProvenTM
Sweat & Water
Resistant
Broad Spectrum
180 ml 

PRINCIPAL DISPLAY PANEL Banana Boat Sport Body and Scalp SPF 30PRINCIPAL DISPLAY PANEL Banana Boat Sport Body and Scalp SPF 30

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17630-2020-12020-01-31C16284748780-19d75b9d0-bed2-f424-e053-dadaa90a57ceBanana Boat Sport Body and Scalp SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17630-2020-1Banana Boat Sport Body and Scalp SPF 30180 mL in 1 BOTTLELOTION1801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17630-2020BANANA BOAT SPORT BODY AND SCALP SPF 30 (HOMOSALATE AND OCTINOXATE AND OCTISALATE AND OCTOCRYLENE AND OXYBENZONE AND AVOBENZONE) LOTION [ACCRA-PAC, INC.]1Legacy NDC, 1 package rows20100330_224060ac-0d53-4b89-8d32-8d28cff7fe3c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
HOMOSALATEACTIVE INGREDIENTV06SV4M95S1
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WM1
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
HOMOSALATEACTIVE MOIETYV06SV4M95S1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
OXYBENZONEACTIVE MOIETY95OOS7VE0Y1
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0X1
AMYL CINNAMALINACTIVE INGREDIENTWC51CA34181
BENZYL BENZOATEINACTIVE INGREDIENTN863NB338G1
C12-15 ALKYL BENZOATEINACTIVE INGREDIENTA9EJ3J61HQ1
CAPRYLYL GLYCOLINACTIVE INGREDIENT00YIU5438U1
GERANIOLINACTIVE INGREDIENTL837108USY1
LIMONENE, DL-INACTIVE INGREDIENT9MC3I344471
LINALOOL, DL-INACTIVE INGREDIENTD81QY6I88E1
VITAMIN A PALMITATEINACTIVE INGREDIENT1D1K0N0VVC1

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17630-202017630-2020-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OXYBENZONE95OOS7VE0YACTIB
AVOBENZONEG63QQF2NOXACTIB
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CAPRYLYL GLYCOL00YIU5438UIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
AMYL CINNAMALWC51CA3418IACT
BENZYL BENZOATEN863NB338GIACT
GERANIOLL837108USYIACT
ALOE VERA LEAFZY81Z83H0XIACT
LIMONENE, DL-9MC3I34447IACT
LINALOOL, DL-D81QY6I88EIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BENZYL BENZOATEBENZYL BENZOATEN863NB338GCAPSULE / ORALNAExact identifier — unii candidate
4 equally ranked IID candidates
BENZYL BENZOATEBENZYL BENZOATEN863NB338GSOLUTION / INTRAMUSCULAR447 mgExact identifier — unii candidate
4 equally ranked IID candidates
BENZYL BENZOATEBENZYL BENZOATEN863NB338GINJECTION / INTRAMUSCULAR1500 mgExact identifier — unii candidate
4 equally ranked IID candidates
BENZYL BENZOATEBENZYL BENZOATEN863NB338GINJECTION, SOLUTION / INTRAMUSCULAR750 mgExact identifier — unii candidate
4 equally ranked IID candidates

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
6704904c-0a25-438d-bebe-f1f10ad01672224060ac-0d53-4b89-8d32-8d28cff7fe3c2010-03-26WarningsExact identifier
spl id: 6704904c-0a25-438d-bebe-f1f10ad01672
spl set id: 224060ac-0d53-4b89-8d32-8d28cff7fe3c

Reported adverse events (FAERS/openFDA)#

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