Banana Boat Sport Performance Active Dry Protect SPF UVB 50

Manufacturer
KIK Custom Products
Effective date
2011-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:28:03

Label at a glance#

ProductBanana Boat Sport Performance Active Dry Protect SPF UVB 50
Active ingredientHomosalate, Octisalate, Octocrylene, Oxybenzone, Avobenzone
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts:

Avobenzone:1.5%
Homosalate: 15%
Octisalate:  5%
Octocrylene: 1.25%
Oxybenzone:  5%


Purpose:  Sunscreen

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT, DO NOT GET INTO EYES IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.
STOP USE AND ASK DOCTOR IS IRRITATION OR RASH DEVELOPS.  KEEP OUT OF REACH OF CHILDREN.
IF SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY.

INACTIVE INGREDIENT SECTION

Water, Stearyl Alcohol, Glycerin, Capryly Glycol, Hydrogenated Dimer, Dilnoleyl Dimethyl Carbonate, Copolymer,
Cetyl Alcohol, Triethanolamine, Behenyl Alcohol, Glyceryl Stearate, Glceryl Stearate Citrate, Disodium, Ethylene,
Dicocamide PEG/15 Disulfate, Sodium Lauryl Sarcosinate, Carbomer, Xanthan Gum, Aloe Barbadenis Leaf Juice, Retinyl Palmitate,
Tocophenol, Tocopheryl Acetate, Cetearyl Alcohol, Sodium Lauryl Lactylate, Leithin, BHT, Methyl Dibromo, Glutaronitrile, Methylchloroisothiazolinone,
Methylisothiazolinone, Phenoxyl Ethanol, Dipropylene Glycol, Disodium EDTA.

OTC - QUESTIONS SECTION

Questions or Comments:  Call 1-800-SAFESUN Mon-Fri.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Tube Label - Back
Image of Tube Label - Back

Image of Tube Label - Front
Image of Tube Label - Front

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.
IF SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY.

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION


Directions:


Apply generously and evenly to all areas 15 minutes before sun exposure.

Re-Apply at frequent intervals and after swimming and towel drying.

Ask a doctor for use on children under 6 months of age.

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61047-831-83Banana Boat Sport Performance Active Dry Protect SPF UVB 50354 mL in 1 BOTTLELOTION3541

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61047-831BANANA BOAT SPORT PERFORMANCE ACTIVE DRY PROTECT SPF UVB 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [KIK CUSTOM PRODUCTS]1Legacy NDC, 1 package rows20110519_d38c97cf-8422-4043-b116-d0b31459dfc7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AvobenzoneACTIVE INGREDIENTG63QQF2NOX1
HomosalateACTIVE INGREDIENTV06SV4M95S1
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
OxybenzoneACTIVE INGREDIENT95OOS7VE0Y1
AvobenzoneACTIVE MOIETYG63QQF2NOX1
HomosalateACTIVE MOIETYV06SV4M95S1
OctisalateACTIVE MOIETY4X49Y0596W1
OctocryleneACTIVE MOIETY5A68WGF6WM1
OxybenzoneACTIVE MOIETY95OOS7VE0Y1
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61047-83161047-831-83

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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 · 6 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL, FOAM / TOPICAL72 mgExact identifier — unii candidate
6 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
352d444d-a1d4-4a9f-9d60-c3f4eac4f165d38c97cf-8422-4043-b116-d0b31459dfc72011-05-18WarningsExact identifier
spl id: 352d444d-a1d4-4a9f-9d60-c3f4eac4f165
spl set id: d38c97cf-8422-4043-b116-d0b31459dfc7

Reported adverse events (FAERS/openFDA)#

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