BANANA BOAT- zinc oxide lotion

Banana Boat by

Drug Labeling and Warnings

Banana Boat by is a Otc medication manufactured, distributed, or labeled by Edgewell Personal Care Brands LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc Oxide 19%

Purpose

Sunscreen

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.

Warnings

For external use only.

May stain some fabrics.

Do not use

on damaged or broken skin.

When using this product

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash occurs.

Keep out of reach of children

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Shake well Apply liberally 15 minutes before sun exposure 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

Water, Isohexadecane, Ethylhexyl Palmitate, Diisopropyl Adipate, Cocos Nucifera (Coconut) Oil, Stearyl/Octyldodecyl Citrate Crosspolymer, Glycerin, Polyhydroxystearic Acid, Silica, Sodium Chloride, Phenoxyethanol, Triethoxycaprylylsilane, Xanthan Gum, Cetyl PEG/PPG10/1 Dimethicone, Caprylyl Glycol, Lauryl PEG-8 Dimethicone, Ethylhexylglycerin, Sodium Citrate, Mica, Tocopheryl Acetate, Titanium Dioxide, Iron Oxides.

Other information

Protect the product in this container from excessive heat and direct sun

Questions or comments?

Call 1-800-SafeSun, Mon-Fri

Principal Display Panel

NEW!
Fast Rub In
BANANA BOAT
SPORT
mineral
100% MINERAL BASED SUNSCREEN LOTION
UVA/UVB BROAD SPECTRUM, SPF 50
50
BLENDS IN ACROSS
SKIN TONES
SWEAT | WATER
RESISTANT
(80 minutes)
5 FL. OZ. (147 mL)

New & Improved
NEW! Fast Rub In
BANANA BOAT
SPORT
mineral
100% MINERAL BASED SUNSCREEN LOTION
UVA/UVB BROAD SPECTRUM, SPF 50
50
BLENDS IN ACROSS
SKIN TONES
SWEAT | WATER
RESISTANT
(80 minutes)
5 FL. OZ. (147 mL)

Carton

50

PROTECTS UP TO 98%

100% MINERAL ACTIVES

WITH NATURALLY

SOURCED ZINC

2 PACK

50

100%

MINERAL

QUICKLY

BLENDS IN

ACROSS ALL SKIN TONES

HIGH

PERFORMANCE

VS. SWEAT & WATER

(80 MINUTES)

DERMATOLOGIST

TESTED

2 - 5 FL. OZ (147 mL)

Tubes, Total 10 FL OZ.

(294 mL)

INGREDIENTS AND APPEARANCE

BANANA BOAT 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-374
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	19 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ISOHEXADECANE (UNII: 918X1OUF1E)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
LAURYL PEG-8 DIMETHICONE (300 CPS) (UNII: ELL2U7K8T8)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
COCONUT OIL (UNII: Q9L0O73W7L)
STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: PN88NW0KPK)
MICA (UNII: V8A1AW0880)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
XANTHAN GUM (UNII: TTV12P4NEE)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-374-23	147 g in 1 TUBE; Type 0: Not a Combination Product	10/01/2024
2	NDC: 63354-374-27	294 g in 1 TUBE; Type 0: Not a Combination Product	10/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/01/2024

Labeler - Edgewell Personal Care Brands LLC (151179769)