SunBum SPF 15

Manufacturer
Sun Bum | Product Quest Mfg.
Effective date
2016-05-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:26:20

Label at a glance#

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

Dosage and administration

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, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: • limit time ...

Label contents#

Full prescribing information#

Active ingredients                        Purpose

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.00%                        Sunscreen
Homosalate 5.00%
Octisalate 2.00%
Octocrylene 1.85%
Oxybenzone 3.00%

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.

Warnings

WARNINGS SECTION

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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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, 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

Behenyl Alcohol
BHT
Butyloctyl Salicylate
Caprylyl Methicone
Dimethicone
Dimethyl Capramide
Disodium EDTA
Ethylhexyl Stearate
Ethylhexylglycerin
Fragrance
Glyceryl Stearate
Hydrated Silica
Methylisothiazolinone
PEG-100 Stearate
Polyaminopropyl Biguanide
Polyester-8
Sodium Polyacrylate
Styrene/Acrylates Copolymer
Tocopheryl Acetate
Trideceth-6
Trimethylsiloxysilicate
VP/Hexadecene Copolymer
Water
Xanthan Gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

FDA-Initiated Inactive NDC Indexing#

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69039-55169039-551-05, 69039-551-03, 69039-551-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
739dca98-fceb-45f9-b0d2-eaf2e4429860eafe23db-36e9-4348-8c82-bf710eca4ff62016-05-03WarningsExact identifier
spl id: 739dca98-fceb-45f9-b0d2-eaf2e4429860
spl set id: eafe23db-36e9-4348-8c82-bf710eca4ff6

Reported adverse events (FAERS/openFDA)#

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