FDA.reportPublic FDA data

Banana Boat KiDS mineral foam Sunscreen Broad Spectrum SPF 50 Plus Berry Blast

Manufacturer
Edgewell Personal Care Brands LLC
Effective date
2023-11-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:19:57

Label at a glance#

ProductBanana Boat KiDS mineral foam Sunscreen Broad Spectrum SPF 50 Plus Berry Blast
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
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 • Dispense in upright position for optimal results • Hold container 4 to 6 inches from the skin to apply • spray liberally and spread evenly by hand 15 minutes before sun exposure • Do 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 • ...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 4.9%, Zinc Oxide 7.1%

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 - Do not consume.

May stain or damage some fabrics or surfaces

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

OTC - STOP USE SECTION

if 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 • Dispense in upright position for optimal results • Hold container 4 to 6 inches from the skin to apply • spray liberally and spread evenly by hand 15 minutes before sun exposure • Do 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

• 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 • Children under 6 months: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isobutane, Caprylic/Capric Triglyceride, Isohexadecane, Butyloctyl Salicylate, Cetyl PEG/PPG-10/1 Dimethicone, Lauryl PEG-8 Dimethicone, VP/Eicosene Copolymer, Sodium Chloride, Ethylhexyl Methoxycrylene, Dimethicone, Polyhydroxystearic Acid, Phenoxyethanol, Caprylyl Glycol, PEG-8, Alumina, Glycerin, Fragrance, Sodium Citrate, Tocopheryl Acetate, Green 6

Other information

SPL UNCLASSIFIED SECTION

• protect this product from excessive heat and direct sun

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-SafeSun, Mon-Fri

Primary Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VANISHING BLUE FOAM

RUBS IN CLEAR

BANANA

BOAT (R)

KiDS

mineral foam

SUNSCREEN LOTION

UVA/UVB BROAD SPECTRUM SPF 50+

50+

BERRY

BLAST*

Water

Resistant

(80 min.)

NET WT 4 OZ. (113g)

63354-666-3363354-666-33

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63354-66663354-666-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
ISOHEXADECANE918X1OUF1EIACT
VINYLPYRROLIDONE/EICOSENE COPOLYMER035MV9S1C3IACT
SODIUM CHLORIDE451W47IQ8XIACT
DIMETHICONE92RU3N3Y1OIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ALUMINUM OXIDELMI26O6933IACT
D&C GREEN NO. 64QP5U84YF7IACT
ZINC OXIDESOI2LOH54ZACTIB
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM CITRATE1Q73Q2JULRIACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)V2W71V8T0XIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
GLYCERINPDC6A3C0OXIACT
ISOBUTANEBXR49TP611IACT
LAURYL PEG/PPG-18/18 METHICONEZJ5S27D9NXIACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT

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
0b390d67-dce4-db5e-e063-6394a90ab9a5b8bae5d9-18b1-8358-e053-2a95a90a35f02023-11-28WarningsExact identifier
spl id: 0b390d67-dce4-db5e-e063-6394a90ab9a5
spl set id: b8bae5d9-18b1-8358-e053-2a95a90a35f0

Reported adverse events (FAERS/openFDA)#

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