Hawaiian Tropic

Manufacturer
Edgewell Personal Care Brands LLC
Effective date
2025-08-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:11:30

Label at a glance#

ProductHawaiian Tropic
Active ingredientHOMOSALATE, OCTOCRYLENE, AVOBENZONE
Label structure14 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

Hold container 4 to 8 inches from the skin to apply. Don't spray directly into face. Apply on hand then apply to face. Spray evenly and liberatly on your skin. Apply 15 minutes before sun exposure. Reapply throughout the day. • at least every 2 hours • after 80 minutes of swimming or sweating • immediately after towel drying • Sun Protection Measures . Spending time in the sun increases your risk of skin cancer an...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.7%, Homosalate 6.0%, Octocrylene 6.0%

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

Flammable

WARNINGS AND PRECAUTIONS SECTION

Do not use in the presence of a flame or spark. Keep away from sources of ignition - No smoking.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

Keep away from face to avoid breathing it. 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.

Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

May stain some fabrics.

Directions

DOSAGE & ADMINISTRATION SECTION

Hold container 4 to 8 inches from the skin to apply. Don't spray directly into face. Apply on hand then apply to face. Spray evenly and liberatly on your skin. Apply 15 minutes before sun exposure. Reapply throughout the day. • at least every 2 hours • after 80 minutes of swimming or sweating • immediately after towel drying • 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

Alcohol Denat., Isododecane, Diisopropyl Adipate, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Caprylyl Glycol, Dimethicone, Fragrance, Camellia Sinensis Leaf Extract

Other Information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-800-NO UV RAY, Mon-Fri

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAWAIIAN

Tropic(R)

AntiOxidant+

REFRESH SUNSCREEN MIST

Helps prevent skin damage

& skin aging from the sun

30

SPF 30 BROAD SPECTRUM SUNSCREEN SPRAY

UVA & UVB PROTECTION

Good for FACE and BODY

lightweight & oil-free formula

with green tea extract

Recommended as an

effective broad spectrum

sunscreen

3.4 FL OZ (100 mL)

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63354-83263354-832-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
3cf77001-59b0-69f5-e063-6394a90a0b617885f941-94f0-c936-e053-2991aa0acba52025-08-22WarningsExact identifier
spl id: 3cf77001-59b0-69f5-e063-6394a90a0b61
spl set id: 7885f941-94f0-c936-e053-2991aa0acba5

Reported adverse events (FAERS/openFDA)#

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