Banana Boat Ultra Defence SPF 30 for UK

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 22:24:02

Label at a glance#

ProductBanana Boat Ultra Defence SPF 30 for UK
Active ingredientHOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, AVOBENZONE
Label structure6 sections

Dosage and administration

Apply generously and evenly to all areas 20 minutes before sun exposure. No need to rub in. Reapply frequently to maintain protection and also after swimming and towel drying. Do not spray directly on face. Spray on hands to apply to face. Use in a well-ventilated area. For external use only. Avoid contact with eyes and clothes.

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 to all areas 20 minutes before sun exposure. No need to rub in. Reapply frequently to maintain protection and also after swimming and towel drying. Do not spray directly on face. Spray on hands to apply to face. Use in a well-ventilated area. For external use only. Avoid contact with eyes and clothes.

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

WARNING:

WARNINGS SECTION

FLAMMABLE. Pressurised container. Protect from sunlight and do not expose to temperatures exceeding 50°C. Do not pierce or burn, even after use. Do not spray on a naked flame, onto or near fire, or any incandescent material. Keep away from sources of ignition – No smoking. Use only as directed.

INGREDIENTS:

INACTIVE INGREDIENT SECTION

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

CLEAR
UltraMist®
BANANA

BOAT
®
Ultra

Defence
ADVANCED
AvoTriplex® UVA & UVB SUN PROTECTION
SPF 30 UVA

AvotriplexTM
High Protection

Sun-Tested, Sun-
ProvenTM
Protects & Cools, Rub-Free

Enriched with Aloe Vera

Very Water Resistant

175 ml

PRINCIPAL DISPLAY PANEL Banana Boat Ultra Defence SPF 30 for UKPRINCIPAL DISPLAY PANEL Banana Boat Ultra Defence SPF 30 for UK

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17630-2022-12020-01-31C16284748780-19d75b9cf-d514-f424-e053-dadaa90a57ceBanana Boat Ultra Defence SPF 30 for UK

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17630-2022-1Banana Boat Ultra Defence SPF 30 for UK175 mL in 1 CANSPRAY1751

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17630-2022BANANA BOAT ULTRA DEFENCE SPF 30 FOR UK (HOMOSALATE AND OCTINOXATE AND OCTISALATE AND OCTOCRYLENE AND OXYBENZONE AND AVOBENZONE) SPRAY [ACCRA-PAC, INC.]1Legacy NDC, 1 package rows20100330_7a5f0733-45ee-4402-b622-214ab0661e29.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
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 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17630-202217630-2022-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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 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
BENZYL BENZOATEBENZYL BENZOATEN863NB338GSOLUTION / INTRAMUSCULAR447 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
fa29e200-6cd5-459e-858d-c04045d0ab047a5f0733-45ee-4402-b622-214ab0661e292010-03-26WarningsExact identifier
spl id: fa29e200-6cd5-459e-858d-c04045d0ab04
spl set id: 7a5f0733-45ee-4402-b622-214ab0661e29

Reported adverse events (FAERS/openFDA)#

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