Ulta

Manufacturer
Prime Enterprises, Inc.
Effective date
2021-04-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:43:24

Label at a glance#

ProductUlta Broad Spectrum SPF 30
Active ingredientHOMOSALATE, AVOBENZONE, OCTISALATE, OCTOCRYLENE
Label structure9 sections

Indications and uses

helps prevent sunburn if use 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

apply liberally 15 minutes before sun exposure. reapply: after 40 mins 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, regulary use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: limit time in the sun, esp...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 7.5%, Octisalate 5%, Octocrylene 5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

helps prevent sunburn

if use 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.

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.

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.

Flammable:

OTHER SAFETY INFORMATION

Do not use near heat, flame or while smoking.

Directions

DOSAGE & ADMINISTRATION SECTION

apply liberally 15 minutes before sun exposure.

reapply: after 40 mins 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, regulary use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:

limit time in the sun, espescially from 10 a.m. - 2p.m.

wear long sleeve shirts, pants, hats, and sunglasses

children under 6 months: Ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Isododecane, Ethylene/Propylene/Styrene Copolymer, Butylene/Ethylene/Styrene Copolymer, Fragrance, Phenoxyethanol, Mica, Iron Oxides, Cocos Nucifera (Coconut) Oil, Titanium Dioxide, Ethylhexylglycerin, Euterpe Oleracea Fruit Oil, Gossypium Herbaceum (Cotton) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Theobroma Grandiflorum Seed Butter, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract, Alumina

Other information:

SPL UNCLASSIFIED SECTION

protect this product from excessive heat and direct sun

avoid spraying on fabrics - could cause discoloration

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-866-983-8582

Ulta Beauty Illuminating Bronzing Oil Broad Spectrum SPF 30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display LabelPrincipal Display Label

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58443-039458443-0394-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
bf3a962f-13c6-58e2-e053-2995a90ab7f4bf3ac08b-a314-5915-e053-2a95a90a79ef2021-04-05WarningsExact identifier
spl id: bf3a962f-13c6-58e2-e053-2995a90ab7f4
spl set id: bf3ac08b-a314-5915-e053-2a95a90a79ef

Reported adverse events (FAERS/openFDA)#

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