FDA.reportPublic FDA data

Banana Boat Natural Reflect Sunscreen Lotion SPF 50+

Manufacturer
Energizer Personal Care LLC | Formulated Solutions, LLC
Effective date
2011-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:49:54

Label at a glance#

ProductBanana Boat Natural Reflect Sunscreen SPF 50 Plus
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure14 sections

Indications and uses

helps prevent sunburn

Dosage and administration

apply generously and evenly to all areas 15 minutes before sun exposure massage in for a clear finish 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#

SPL UNCLASSIFIED SECTION

Banana Boat Lotion Natural Reflect SPF 50+  provides clinically proven protection against sunburn and long-term skin damage without the use of harsh chemical sunscreens because it is formulated with 100% naturally-sourced sunscreen actives. After rubbing in, this rich, more natural mineral sunscreen feels clean on your skin and provides a clear protective layer that reflects UVA and UVB rays. It is Dermatologist-tested and gentle enough for use on sensitive skin.

  • Oxybenzone-Free
  • Oil-Free
  • UVA/UVB Protection
  • Leaves no white residue

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 2.8%, Zinc Oxide 4.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of contact rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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
  • massage in for a clear finish
  • reapply at frequent intervals and after swimming or towel drying
  • ask a doctor before use on children under six months of age

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Phenethyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Lauryl PEG-8 Dimethicone, Ozokerite, Cyclopentasiloxane, Cyclohexasiloxane, C30-38 Olefin/Isopropyl Maleate/MA Copolymer, Ethylhexyl Methoxycrylene, PEG-8, Sodium Chloride, Caprylyl Glycol, Dimethicone, Glycerin, Sodium Citrate, Disodium EDTA, Panthenol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice (Aloe Vera), Phenoxyethanol.

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.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-800-SafeSun, Mon-Fri

SPL UNCLASSIFIED SECTION

The Skin Cancer Foundation recommends this product as an effective UV sunscreen.

www.bananaboat.com

MADE IN U.S.A.

Dist. By:

ENERGIZER PERSONAL CARE, LLC

SHELTON, CT 06484

2011 Sun Pharmaceuticals, LLC

Banana Boat Natural Reflect Sunscreen Lotion SPF 50+

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW!

BANANA BOAT

natural

reflect

sunscreen lotion

SPF 50+

BROAD SPECTRUM

100% Naturally Sourced Sunscreens with Zinc Oxide

Proven Effective Against Sunburn and Long-Term Damage

Paraben and PABA Free

Very Water Resistant

4 FL. OZ. (118 ml)

RECOMMENDED

SKIN CANCER FOUNDATION

ACTIVE



Label 1Label 1

Label 2Label 2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130079656051421GTIN-13: 0079656051421
EAN-13: 0079656051421
GTIN-12: 079656051421
UPC-A: 079656051421
GTIN storage (14 digits): 00079656051421		BBSPF50B.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63354-001-002020-01-31C16284748780-19d75b9cf-daa2-f424-e053-dadaa90a57ceBanana Boat Natural Reflect Sunscreen Lotion SPF 50+

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63354-00163354-001-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
ISOHEXADECANE918X1OUF1EIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5)035JKJ76MTIACT
ISOPROPYL MALEATEM86R5J916VIACT
SODIUM CHLORIDE451W47IQ8XIACT
DIMETHICONE92RU3N3Y1OIACT
CAPRYLYL GLYCOL00YIU5438UIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
ALUMINUM OXIDELMI26O6933IACT
GLYCERINPDC6A3C0OXIACT
SODIUM CITRATE1Q73Q2JULRIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
EDETATE DISODIUM7FLD91C86KIACT
PANTHENOLWV9CM0O67ZIACT

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
643c11ac-3188-4433-abb5-b7b2f0d528ae1379a789-b6d8-4173-8bf8-4f128435829a2011-12-29WarningsExact identifier
spl id: 643c11ac-3188-4433-abb5-b7b2f0d528ae
spl set id: 1379a789-b6d8-4173-8bf8-4f128435829a

Reported adverse events (FAERS/openFDA)#

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