FDA.reportPublic FDA data

Wild Tropics D49.000/D49AA Sunscreen Spray SPF 50

Manufacturer
Consumer Product Partners, LLC
Effective date
2024-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:10:40

Label at a glance#

ProductSunscreen SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE
Label structure15 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

■ spray liberally and spread evenly by hand 15 minutes before sun exposure ■ apply to all skin exposed to the sun ■ hold container 4 to 6 inches from the skin to apply ■ do not spray directly into face. Spray on hands then apply to face. ■ do not apply in windy conditions ■ use in a well-ventilated area and avoid inhalation ■ reapply: ■ after 80 minutes of swimming or sweating ■ immediately after towel drying ■ at...

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 12%

Octisalate 5%

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

SPL UNCLASSIFIED SECTION

  • Flammable: keep away from fire or flame. 
  • After application, wait until product dries before approaching a source of heat or flame, or before smoking

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
  • contents under pressure.  Do not puncture or incinerate.  Do not store at temperature above 120°F

Stop use and ask a doctor if 

OTC - STOP USE SECTION

rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek immediate medical attention or call a poison control center.

Directions

DOSAGE & ADMINISTRATION SECTION

■ spray liberally and spread evenly by hand 15 minutes before sun exposure
■ apply to all skin exposed to the sun
■ hold container 4 to 6 inches from the skin to apply
■ do not spray directly into face. Spray on hands then apply to face.
■ do not apply in windy conditions
■ use in a well-ventilated area and avoid inhalation
■ 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 of age: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., diethylhexyl 2,6-naphthalate, diisopropyl adipate, acrylates/octylacrylamide copolymer, butyloctyl salicylate, neopentyl glycol diheptanoate, fragrance, tocopheryl acetate

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by Sun Bum LLC, distributor of Sun Bum® Premium Moisturizing Sunscreen Spray Broad Spectrum SPF 50.

May stain or damage some fabrics or surfaces

Adverse Reaction

ADVERSE REACTIONS SECTION

Manufactured by: Vi-Jon, LLC

One Swan Drive

Smyrna, TN 37167

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

wild tropics ™

SUNSCREEN SPRAY

BROAD SPECTRUM SPF 50

HYPOALLERGENIC

DERMATOLOGIST TESTED

WATER RESISTANT (80 MINUTES)

FRESH BANANA SCENT

Compare to Sun Bum® Premium Moisturizing Sunscreen Spray*

SPF 50

NET WT 5.5 OZ (156 g)

image descriptionimage description

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11344-049SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE) SPRAY [CONSUMER PRODUCT PARTNERS, LLC]1Unmatched20240302_f5217655-6fb4-4757-91cd-bbe154ba9d62.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11344-04911344-049-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW)7LL6SY9YFVIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB

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
38e33e4b-336e-b355-e063-6294a90a04a5f5217655-6fb4-4757-91cd-bbe154ba9d622025-07-01Warnings, Adverse reactionsExact identifier
spl set id: f5217655-6fb4-4757-91cd-bbe154ba9d62

Reported adverse events (FAERS/openFDA)#

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