SPF 50 Sunscreen Spray 055.000/055AA

Manufacturer
Vi-Jon, LLC
Effective date
2022-09-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:53:28

Label at a glance#

ProductSunscreen
Active ingredientAvobenzone, Homosalate, Octisalate, OCTOCRYLENE
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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone, Homosalate, Octisalate, Octocrylene

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

Keep away from fire or flame.

  • after application, wait until product dries before approacing a souce 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 120ºF.

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, get medical help or contact a Poison Conrol Center right away

Direction

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

INACTIVE INGREDIENT SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., acrylates/octylacrylamide copolymer, glycerin, triethanolamine, tocopherol, butyloctyl salicylate, fragrance

SPL UNCLASSIFIED SECTION

May stain or damage some fabrics of surfaces

Oxybenzone & Octinoxate free

This product is not manufactured or distributed by S.C. Johnson & Sons, Inc., distributor of Sun Burn Premium Moisturizing Sunscreen Spray Broad Spectrum SPF 50.

DISTRUBUTED BY DOLGENCORP, LLC

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

100% Satisfaction Guaranteed! (888)309-9030

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Wild

Tropics

SUNSCREEN

SPRAY

BROAD SPECTRUM SPF 50

OCTINOXAQTE & OXYBENZONE FREE

HYPOALLERGENIC

DERMATP;PGOST TESTED

WATER RESISTANT (80 MINUTES)

FRESH BANANA SCENT

Compare to Sun Bum Premium

Moiturizing Sunscreen Spray

SPF

50

NET WT 5.5 OZ (156 g)

image descriptionimage description

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
0869-00550869-0055-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
147ff593-8aa9-8eeb-e063-6394a90a7781ee3a23b3-189a-43de-b638-cecc0993e3f22024-03-25WarningsExact identifier
spl set id: ee3a23b3-189a-43de-b638-cecc0993e3f2

Reported adverse events (FAERS/openFDA)#

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