TITANIUM DIOXIDE

Manufacturer
Laboratoires Clarins
Effective date
2019-12-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:47:57

Label at a glance#

ProductCLARINS - SKIN ILLUSION - BROAD SPECTRUM SPF 15 - TITANIUM DIOXIDE - SUNSCREEN - Natural Hydrating Foundation 101
Active ingredientTITANIUM DIOXIDE
Label structure8 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.

Dosage and administration

apply liberally 15 minutes before sun exposure apply to all skin exposed to the sun  children under 6 months: Ask a doctor 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. - ...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

TITANIUM DIOXIDE 2.8%

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.

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 if

OTC - STOP USE SECTION

  • 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.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • apply to all skin exposed to the sun 
  • children under 6 months: Ask a doctor
  • 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-sleeved shirts, pants, hats and sunglasses.
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA/WATER/EAU, METHYL TRIMETHICONE, DIMETHICONE, ALCOHOL, ISODODECANE, BUTYLENE GLYCOL, PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, GLYCERIN, DIMETHICONE/PEG-10/15 CROSSPOLYMER, POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, SODIUM CHLORIDE, SQUALANE, ALUMINUM HYDROXIDE, STEARIC ACID, PARFUM/FRAGRANCE, SILYBUM MARIANUM SEED OIL, DISTEARDIMONIUM HECTORITE, PROPYLENE CARBONATE, ETHYLHEXYLGLYCERIN, TOCOPHERYL ACETATE, TRIETHOXYCAPRYLYLSILANE, DISODIUM EDTA, HYDROXYETHYL UREA, SYNTHETIC FLUORPHLOGOPITE, DIPROPYLENE GLYCOL, KALANCHOE PINNATA LEAF EXTRACT, PHENOXYETHANOL, ALGIN, SODIUM CITRATE, CITRIC ACID, ACACIA SENEGAL GUM, JANIA RUBENS EXTRACT, FURCELLARIA LUMBRICALIS EXTRACT, SODIUM BENZOATE, POTASSIUM SORBATE, CAMELLIA SINENSIS LEAF EXTRACT, TOCOPHEROL, LAPSANA COMMUNIS FLOWER/LEAF/STEM EXTRACT, MARIS SAL/SEA SALT, SEL MARIN, +/- MAY CONTAIN/PEUT CONTENIR: MICA, SILICA, CI 77891/TITANIUM DIOXIDE, CI 77491/CI 77492/CI 77499/IRON OXIDES. [M3012A]

Other information:

SPL UNCLASSIFIED SECTION

  • protect this product from excessive heat and direct sun.

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-866-252-7467 (In the US) Monday-Friday, 8 a.m. to 5 p.m.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package2Outer Package2Inner Package2Inner Package2LabelLabelTESTERTESTERBoxBox

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58668-170158668-1701-1, 58668-1701-2

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d02ae63d-611f-0057-e053-2995a90a633548ebf157-dbcd-4b95-aea2-6530ed4cff282021-11-06WarningsExact identifier
spl set id: 48ebf157-dbcd-4b95-aea2-6530ed4cff28

Reported adverse events (FAERS/openFDA)#

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