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Banana Boat Package Insert

Status:
Prescription (Rx) Facts
Strength:
3.1 g/100 g, 4 g/100 g
Active ingredients:

Prescribing information (package insert) - Banana Boat

Active Ingredients

Titanium Dioxide 3.1%

Zinc Oxide 4.0%

Purpose

Sunscreen

Uses

  • helps prevent sunburn
  • if used as directed wiht 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
  • 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 swallowed, get medical help or contact a Poison Control Center right away.

May stain some fabrics.

Directions

  • 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, regulatory use a sunscreen with a broad spectrum SPF 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-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months: Ask a doctor

Other information

  • protect this product from excessive heat and direct sun

Questions or Comments?

Call 1-800-SafeSun, Mon-Fri

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: OTC MONOGRAPH NOT FINAL 352 · View the label on DailyMed

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Banana Boat

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Active ingredients Titanium dioxide 3.1 g/100 g, Zinc oxide 4 g/100 g
Dosage form Lotion
Route Topical
Marketing status not in the current FDA NDC Directory
Company (applicant) Energizer Personal Care LLC
FDA approval OTC MONOGRAPH NOT FINAL 352OTC monograph
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
3.1 g/100 g, 4 g/100 g – 236 g in 1 tube NDC 63354-050-26
3.1 g/100 g, 4 g/100 g – 295 g in 1 tube NDC 63354-050-27

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.