02 CUSHION SPF45

Manufacturer
COIZ CO LTD | OC QUEST INC
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:57:29

Label at a glance#

Product02 CUSHION SPF45 SUNSCREEN
Active ingredientOCTISALATE, TITANIUM DIOXIDE, OCTOCRYLENE, ZINC OXIDE, OCTINOXATE
Label structure13 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 sun

Dosage and administration

▪ Using puff applicator, press down lightly onto presaturated cushion sponge to capture product. For maximum coverage, pat evenly over face. For light coverage, smooth over face using sweeping motion. ▪ Apply liberally and evenly 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 ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 7.0%

Ethylhexyl Salicylate 5.0%

Octocrylene 2.5%

Titanium Dioxide 13.5%

Zinc Oxide 5.0%

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 sun

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

When using

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help
or contact a Poison Control Center right away.

Directions

INSTRUCTIONS FOR USE SECTION

▪ Using puff applicator, press down lightly onto presaturated cushion sponge to capture product. For maximum coverage, pat evenly over face. For light coverage, smooth over face using sweeping motion.
▪ Apply liberally and evenly 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 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 ▪ Use a water-resistant sunscreen if swimming or sweating.

Other Information

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium chloride, Peg-9 diglycidyl ether/sodium hyaluronate crosspolymer, .Alpha.-Tocopherol acetate, Hamamelis virginiana flower water, Brown iron oxide, Edetate disodium anhydrous, Disteardimonium hectorite, Hexyl Laurate, Ferric oxide red, Cyclomethicone 5, Caprylic / capric / lauric triglyceride, Adenosine, Stearic acid, Glycerin, 1,2-Hexanediol, Aluminium oxide, Ferric oxide yellow, Centella asiatica, Cetyl PEG/PPG-10/1 Dimethicone, Mica, Triethoxycaprylylsilane, Water, Benzyl salicylate, Linalool, Polyhydroxystearic acid (2300 MW), PEG-10 Dimethicone, Oxygen, Hydroxyisohexyl 3-Cyclohexene carboxaldehyde, Dimethicone PEG-8 Laurate, Niacinamide.

Questions or Comments

OTC - QUESTIONS SECTION

Questions or Comments?
Call 1-855-460-6190 or visit www.oxygenceuticals.com

O2 CUSHION SPF 45 SUNSCREEN 30 mL (72498-000-01)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Coiz Co Ltd O2 Cushion SunscreenCoiz Co Ltd O2 Cushion Sunscreen

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72498-00072498-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 36 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c7314c70-4fbe-4e8d-e053-2a95a90a36197e7d4f99-2b83-0d1e-e053-2a91aa0aa84d2021-01-01WarningsExact identifier
spl set id: 7e7d4f99-2b83-0d1e-e053-2a91aa0aa84d

Reported adverse events (FAERS/openFDA)#

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