Lancome UV Expert Mineral CC Cream with Titanium Dioxide SPF 50 Color Correcting

Manufacturer
L'Oreal USA Products Inc | SICOS ET CIE
Effective date
2023-01-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:38:57

Label at a glance#

ProductLancome UV Expert Mineral CC Cream with Titanium Dioxide SPF 50 Color Correcting
Active ingredientTITANIUM DIOXIDE
Label structure12 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin caner and early skin aging caused by the sun

Dosage and administration

For sunscreen use: apply generously and evenly 15 minutes before sun exposure reapply at least every 12 hours use a water resistant sunscreen if swimming or sweating 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 of 15 or higher and other sun protection measures including:         * limit time in the sun, e...

Storage and handling

protect the product in this container from excessive heat and direct sun

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 15.5%

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

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

  • apply generously and evenly 15 minutes before sun exposure
  • reapply at least every 12 hours
  • use a water resistant sunscreen if swimming or sweating
  • 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 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

  • children under 6 months of age: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, diisopropyl sebacate, glycerin, alcohol denat., isopropyl palmitate, caprylic/capric triglyceride, propanediol, diethylhexyl syringylidenemalonate, polyglyceryl-6 polyricinoleate, isocetyl stearate, aluminum hydroxide, stearic acid, tocopherol, sodium benzoate, stearalkonium hectorite, triethoxysilylethyl polydimethylsiloxyethyl dimethicone, polyhydroxystearic acid, maltodextrin, xanthan gum, pentylene glycol, mentha piperita (peppermint) extract, isopropyl titanium triisostearate, propylene glycol, leontopodium alpinum flower/leaf extract, caprylyl glycol, moringa oleifera seed extract, sorbitol, rosa gallica flower extract, citric acid, potassium sorbate, aluminum stearate, alumina, fragrance: may contains iron oxides, titanium dioxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a cartonimage of a carton

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-22649967-226-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML · Source PDF

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
eb4deb4d-2b61-4b6b-969a-22d11d88d889658083ed-ef9e-444c-b53c-dbc797a869812023-01-24WarningsExact identifier
spl id: eb4deb4d-2b61-4b6b-969a-22d11d88d889
spl set id: 658083ed-ef9e-444c-b53c-dbc797a86981

Reported adverse events (FAERS/openFDA)#

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