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Drug Facts

Manufacturer
L'Oreal USA Products Inc | SICOS ET CIE
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:19:27

Label at a glance#

ProductLancome Paris Teint Visionnaire Skin Correcting Makeup Duo Foundation Broad Spectrum SPF 20
Active ingredientOCTINOXATE
Label structure14 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

For sunscreen use: ● apply liberally 15 minutes before sun exposure ● reapply at least every 2 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 with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: ● limit...

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.5%

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 cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Flammable until dry.

SAFE HANDLING WARNING SECTION

Do not use near fire, flame or heat.

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

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

● apply liberally 15 minutes before sun exposure

● reapply at least every 2 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 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

● 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, dimethicone, phenyl trimethicone, cyclohexasiloxane, propanediol, butylene glycol, alcohol denat., cetyl PEG/PPG-10/1 dimethicone, sodium tetrahydrojasmonate, synthetic fluorphlogopite, dipropylene glycol, polyglyceryl-4 isosearate, PEG/PPG-18/18 dimethicone, sorbitol, dimethicone/PEG-10/15 crosspolymer, dimethicone/polyglycerin-3 crosspolymer, aluminum hydroxide, adenosine, magnesium sulfate, disodium stearoyl glutamate, acrylates copolymer, phenoxyethanol; may contain: titanium dioxide, bismuth oxychloride, iron oxides, ferric ammonium ferrocyanide

Questions or comments?

OTC - QUESTIONS SECTION

1-800-LANCOME (1-800-526-2663)

Monday - Friday (9 a.m. - 5 p.m. EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
OCTINOXATEACTIVE MOIETY4Y5P7MUD512

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-20549967-205-01, 49967-205-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
CYCLOMETHICONE 6XHK3U310BAIACT
PROPANEDIOL5965N8W85TIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALCOHOL3K9958V90MIACT
DIPROPYLENE GLYCOLE107L85C40IACT
POLYGLYCERYL-4 ISOSTEARATE820DPX33S7IACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
SORBITOL506T60A25RIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
ADENOSINEK72T3FS567IACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
DISODIUM STEAROYL GLUTAMATE45ASM2L11MIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
BISMUTH OXYCHLORIDE4ZR792I587IACT
FERRIC OXIDE RED1K09F3G675IACT
FERRIC AMMONIUM FERROCYANIDE9R0NVI936IIACT

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
bcde2b81-c875-4b23-a8fa-10780f7a6f20d9cd7627-efb8-49f8-bca2-2b28da8bc7042023-01-24WarningsExact identifier
spl set id: d9cd7627-efb8-49f8-bca2-2b28da8bc704

Reported adverse events (FAERS/openFDA)#

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