VALENTINO VERY VALENTINO LIGHT LASTING PERFECTING FOUNDATION BROAD SPECTRUM SPF 26 SUNSCREEN- octinoxate and titanium dioxide lotion

Valentino Very Valentino Light Lasting Perfecting Foundation Broad Spectrum SPF 26 Sunscreen by

Drug Labeling and Warnings

Valentino Very Valentino Light Lasting Perfecting Foundation Broad Spectrum SPF 26 Sunscreen by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, SICOS ET CIE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Octinoxate 6.7%

Titanium dioxide 1.8%

Purpose

Sunscreen

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

Warnings

For external use only

Flammable until dry.

Do not use near fire, flame or heat.

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 before use

● apply generously 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, dimethicone, isododecane, alcohol denat., trimethylsiloxysilicate, butylene glycol,, PEG-10 dimethicone, synthetic fluorphlogopite, phenyl trimethicone, glycerin, perlite, isopropyl lauroyl sarcosinate, diisopropyl sebacate, disteardimonium hectorite, HDI/trimethylol hexyllactone crosspolymer, bis-PEG/PPG-14/14 dimethicone, magnesium sulfate, phenoxyethanol, disodium stearoyl glutamate, aluminum hydroxide, dipentaerythrityl tetrahydroxystearate/tetraisostearate, hydrogen dimethicone, fragrance, silica silylate, magnesium silicate, silica, linalool, limonene, BHT, citrus aurantium bergamia (bergamot) fruit oil, tin oxide, citronellol, benzyl alcohol; may contain: titanium dioxide, iron oxides, bismuth oxychloride

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VALENTINO VERY VALENTINO LIGHT LASTING PERFECTING FOUNDATION BROAD SPECTRUM SPF 26 SUNSCREEN 
octinoxate and titanium dioxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-180
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	67 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	18 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISODODECANE (UNII: A8289P68Y2)
ALCOHOL (UNII: 3K9958V90M)
TRIMETHYLSILOXYSILICATE (M/Q 0.8-1.0) (UNII: 25LXE464L2)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
GLYCERIN (UNII: PDC6A3C0OX)
PERLITE (UNII: 0SG101ZGK9)
ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J)
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
DIPENTAERYTHRITYL TETRAHYDROXYSTEARATE/TETRAISOSTEARATE (UNII: 230K0823CE)
HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
MAGNESIUM SILICATE (UNII: 9B9691B2N9)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
BERGAMOT OIL (UNII: 39W1PKE3JI)
STANNIC OXIDE (UNII: KM7N50LOS6)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
BENZYL ALCOHOL (UNII: LKG8494WBH)
FERRIC OXIDE RED (UNII: 1K09F3G675)
BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-180-01	1 in 1 CARTON	02/01/2021
1		25 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 49967-180-02	1 mL in 1 PACKET; Type 0: Not a Combination Product	02/01/2021
3	NDC: 49967-180-03	1 in 1 CARTON	02/01/2021
3		5 mL in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 49967-180-04	0.3 mL in 1 PACKET; Type 0: Not a Combination Product	02/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/01/2021

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
SICOS ET CIE		276993581	manufacture(49967-180) , pack(49967-180)

Establishment
Name	Address	ID/FEI	Business Operations
SOCOPLAN		276221405	pack(49967-180)