LANCOME PARIS PHOTOGENIC LUMESSENCE LIGHT MASTERING AND LINE SMOOTHING MAKEUP NORMAL TO DRY SKIN BROAD SPECTRUM SPF 15 SUNSCREEN- octinoxate lotion

Lancome Paris Photogenic Lumessence Light Mastering and Line Smoothing Makeup Normal to Dry Skin Broad Spectrum SPF 15 Sunscreen by

Drug Labeling and Warnings

Lancome Paris Photogenic Lumessence Light Mastering and Line Smoothing Makeup Normal to Dry Skin Broad Spectrum SPF 15 Sunscreen by is a Otc medication manufactured, distributed, or labeled by L’Oreal USA Products Inc, L’Oreal USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Octinoxate 5%

Purpose

Sunscreen

Use

• 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

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

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

Directions

For sunscreen use:
● shake well

● 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

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

Inactive ingredients

water, cyclopentasiloxane, dimethicone, glycerin, HDI/trimethylol hexyllactone crosspolymer, PEG-10 dimethicone, dimethicone/PEG-10/15 crosspolymer, dimethicone/polyglycerin-3 crosspolymer, bis-diglyceryl polyacyladipate-2, sodium hyaluronate, aluminum hydroxide, magnesium sulfate, disodium stearoyl glutamate, propylene glycol, citronellol, pentylene glycol, butylphenyl methylpropional, fragrance, hydroxyisohexyl 3-cyclohexene carboxaldehyde, hexyl cinnamal, methylparaben, phenoxyethanol, butylparaben, diazolidinyl urea; may contain: mica, titanium dioxide, iron oxides

Questions or comments?

1-800-LANCOME

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LANCOME PARIS PHOTOGENIC LUMESSENCE LIGHT MASTERING AND LINE SMOOTHING MAKEUP NORMAL TO DRY SKIN BROAD SPECTRUM SPF 15 SUNSCREEN 
octinoxate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-867
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
METHYLPARABEN (UNII: A2I8C7HI9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
MICA (UNII: V8A1AW0880)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-867-01	1 in 1 CARTON	12/23/2010
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	12/23/2010

Labeler - L’Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L’Oreal USA, Inc.		185931458	manufacture(49967-867)