Lancome Bienfait UV SPF 50 Plus Super Fluid Facial Sunscreen

Manufacturer
L'Oreal USA Products Inc | Cosmetic Essence, LLC
Effective date
2018-12-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:12:18

Label at a glance#

ProductLancome Bienfait UV SPF 50 Plus Super Fluid Facial Sunscreen
Active ingredientAvobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Label structure11 sections

Indications and uses

helps prevent sunburn higher SPF gives more sunburn protection retains SPF after 40 minutes of activity in the water or perspiring provides protection from the UVA rays that may contribute to skin damage and premature aging of the skin

Dosage and administration

shake well before use apply evenly before sun exposure reapply as needed or after towel drying, swimming, or perspiring children under 6 months of age: ask a doctor

Storage and handling

Other information store at 20-25o C (68-77oF)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 15%

Octisalate 5%

Octocrylene 5%

Oxybenzone 6%

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • higher SPF gives more sunburn protection
  • retains SPF after 40 minutes of activity in the water or perspiring
  • provides protection from the UVA rays that may contribute to skin damage and premature aging of the skin

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well before use
  • apply evenly before sun exposure
  • reapply as needed or after towel drying, swimming, or perspiring
  • children under 6 months of age: ask a doctor

Warnings

WARNINGS SECTION

For external use only

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 or irritation develops and lasts

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.

Other information

STORAGE AND HANDLING SECTION

Other information

store at 20-25o C (68-77oF)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER
CYCLOPENTASILOXANE
ALCOHOL DENAT.
SILICA
DICAPRYLYL ETHER
STYRENE/ACRYLATES COPOLYMER
PEG-30 DIPOLYHYDROXYSTEARATE
DIMETHICONE
CYCLOHEXASILOXANE
POLYMETHYLSILSESQUIOXANE
NYLON-12
DICAPRYLYL CARBONATE
PHENOXYETHANOL
LAURYL PEG/PPG-18/18 METHICONE
SODIUM CHLORIDE
CAPRYLYL GLYCOL
METHYLPARABEN
POLY C10-30 ALKYL ACRYLATE
DISTEARDIMONIUM HECTORITE
DISODIUM EDTA
DODECENE
POLOXAMER 407

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AvobenzoneACTIVE INGREDIENTG63QQF2NOX1
HomosalateACTIVE INGREDIENTV06SV4M95S1
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
OxybenzoneACTIVE INGREDIENT95OOS7VE0Y1
AvobenzoneACTIVE MOIETYG63QQF2NOX1
HomosalateACTIVE MOIETYV06SV4M95S1
OctisalateACTIVE MOIETY4X49Y0596W1
OctocryleneACTIVE MOIETY5A68WGF6WM1
OxybenzoneACTIVE MOIETY95OOS7VE0Y1

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
49967-54249967-542-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
9fa8a4cf-91ed-4548-8d54-0ab2ec7b7b20a7b1a954-62f8-4f4a-b1a2-34dbe429194e2018-12-27WarningsExact identifier
spl id: 9fa8a4cf-91ed-4548-8d54-0ab2ec7b7b20
spl set id: a7b1a954-62f8-4f4a-b1a2-34dbe429194e

Reported adverse events (FAERS/openFDA)#

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