SunBum SPF 15

Manufacturer
Sun Bum | Product Quest Mfg.
Effective date
2016-08-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:24:39

Label at a glance#

ProductSunBum SPF 15
Active ingredientAvobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Label structure6 sections

Dosage and administration

• Hold container 4-6 inches from skin to apply. • Spray liberally and spread evenly by hands 15 minutes before sun exposure • Do not spray directly into face. Spray on hands then apply to face. • Do not apply in windy conditions. Use in well-ventilated area. • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • Sun Protection Measures. Spending time in th...

Label contents#

Full prescribing information#

Active ingredients                        Purpose

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.00%                        Sunscreen
Homosalate 6.00%
Octisalate 2.00%
Octocrylene 1.85%
Oxybenzone 2.00%

INDICATIONS & USAGE SECTION

Uses

- helps prevent sunburn
- if used as directed with other sun protection messures (see Directions) decreases the risk of skin cancer and early skin aging caused by sun.

WarningsFor external use only

WARNINGS SECTION

Flammable: Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F. Do not use at presence of a flame or spark. Keep away from sources of ignition – No smoking. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

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

DOSAGE & ADMINISTRATION SECTION

• Hold container 4-6 inches from skin to apply.
• Spray liberally and spread evenly by hands 15 minutes before sun exposure
• Do not spray directly into face. Spray on hands then apply to face.
• Do not apply in windy conditions. Use in well-ventilated area.
• 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 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/Dimethicone Copolymer
Acrylates/Octylacrylamide Copolymer
Alcohol Denat.
Ascorbyl Palmitate
Cyclopentasiloxane
Dimethicone
Fragrance
Polyester-8
PPG-5-Ceteth-20
Tocopheryl Acetate
Trisiloxane

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69039-555-052020-02-27C16284748780-19d75b9d0-a53d-f424-e053-dadaa90a57ceDrug Facts
69039-555-052020-01-31C16284748780-19d75b9d0-a53d-f424-e053-dadaa90a57ceDrug Facts

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69039-55569039-555-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
dbe40648-1e7b-4659-a616-47b3d9ef2d7cd3902919-e2cf-4cf3-994b-94c8b43bb28d2016-08-01WarningsExact identifier
spl id: dbe40648-1e7b-4659-a616-47b3d9ef2d7c
spl set id: d3902919-e2cf-4cf3-994b-94c8b43bb28d

Reported adverse events (FAERS/openFDA)#

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