ANTI-AGING DAY SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, octinoxate, octisalate, octocrylene cream

ANTI-AGING DAY SUNSCREEN BROAD SPECTRUM SPF 30 by

Drug Labeling and Warnings

ANTI-AGING DAY SUNSCREEN BROAD SPECTRUM SPF 30 by is a Otc medication manufactured, distributed, or labeled by La Prairie, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 3.0%
Octinoxate 7.5%
Octisalate 5.0%
Octocrylene 2.5%

Purpose

Sunscreen

Uses

helps prevent sunburn

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

Directions:

apply daily after cleansing and toning smooth over face and throat apply liberally 15 minutes before sun exposure children under 6 months of age: Ask a doctor reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increase 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-sleeve shirts, pants, hats and sunglasses

Inactive Ingredients:

Water (Aqua), C12-15 Alkyl Ethylhexanoate, Glycerin, Dimethicone/Vinyl Dimethicone Crosspolymer, Polyglyceryl-3 Methylglucose Distearate, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Steareth-21, Behenyl Alcohol, Butylene Glycol, Glycoproteins*, Panax Ginseng Root Extract*, Equisetum Arvense Extract*, Sodium Hyaluronate, Caprooyl Tetrapeptide-3, Salicornia Herbacea Extract, Sodium PCA, Triacetin, Tocopheryl Acetate, Resveratrol, Lactobacillus Ferment, Acetyl Decapeptide-3, Trehalose, Urea, Larix Sibirica Wood Extract, Palmitoyl Tripeptide-8, Carnosine, Potato Starch Modified, Disodium EDTA , Myrothamnus Flabellifolia Leaf Extract, Kefiran, Sodium Hydroxide, Glyceryl Stearate, Chlorella Vulgaris Extract, Silica, Panthenol, Polyquaternium-51, Glycine Soja (Soybean) Oil, PEG-100 Stearate, Hydrogenated Lecithin, Allantoin, Hydroxyethyl Behenamidopropyl Dimonium Chloride, C13-14 Isoparaffin, Dextran, Caprylic/Capric Triglyceride, Polysorbate 80, Sodium Oleate, Laureth-7, Saccharomyces Cerevisiae Extract, Cetyl Dimethicone, Caprylyl Glycol, Polyquaternium-67, Steareth-2, Polyacrylamide, Carbomer, Synthetic Wax, Alcohol, Fragrance (Parfum), Linalool, Hexyl Cinnamal, Hydroxycitronellal, Alpha-Isomethyl Ionone, Geraniol, Citronellol, Benzyl Benzoate, Butylphenyl Methylpropional, Evernia Furfuracea (Treemoss) Extract, Eugenol, Benzyl Salicylate, Ethylhexylglycerin, Phenoxyethanol, Sorbic Acid, Sodium Dehydroacetate, Chlorphenesin, Methylparaben, Benzoic Acid, Yellow 5 (CI 19140), Red 4 (CI 14700) i73 * La Prairie’s exclusive Cellular Complex US Patent 5,840,309

Other Information

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

Questions or comments?

Call toll free 1-800-821-5718 or visit www.laprairie.com

LABORATOIRES LA PRAIRIE S.A.

CLARENS/MONTREUX ZURICH D-76530 BADEN-BADEN MILANO PARIS LA PRAIRIE, INC., DISTR. NEW YORK, N.Y. 10019

PRINCIPAL DISPLAY PANEL

ANTI-AGING DAY CREAM SUNSCREEN BROAD SPECTRUM CREME DE JOUR ANTI-AGE CREME SOLAIRE LARGE SPECTRE SPF 30 la prairie SWITZERLAND 50 ml e / NET WT. 1.7 OZ. MADE IN SWITZERLAND

Product Labels

INGREDIENTS AND APPEARANCE

ANTI-AGING DAY SUNSCREEN BROAD SPECTRUM SPF 30 
avobenzone, octinoxate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68026-503
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
C12-15 ALKYL ETHYLHEXANOATE (UNII: GQJ580CH83)
GLYCERIN (UNII: PDC6A3C0OX)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
STEARETH-21 (UNII: 53J3F32P58)
DOCOSANOL (UNII: 9G1OE216XY)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ASIAN GINSENG (UNII: CUQ3A77YXI)
EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CAPROOYL TETRAPEPTIDE-3 (UNII: LZI0HJ3K2R)
SALICORNIA EUROPAEA (UNII: 6ADL50JAKW)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
TRIACETIN (UNII: XHX3C3X673)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
RESVERATROL (UNII: Q369O8926L)
LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
ACETYL DECAPEPTIDE-3 (UNII: 30510A08G7)
TREHALOSE (UNII: B8WCK70T7I)
UREA (UNII: 8W8T17847W)
LARIX SIBIRICA WOOD (UNII: KSC3PGF73L)
CARNOSINE (UNII: 8HO6PVN24W)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
MYROTHAMNUS FLABELLIFOLIA LEAF (UNII: 6Y9E0R40J5)
KEFIRAN (UNII: 8L821V6V99)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CHLORELLA VULGARIS (UNII: RYQ4R60M02)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PANTHENOL (UNII: WV9CM0O67Z)
SOYBEAN OIL (UNII: 241ATL177A)
PEG-100 STEARATE (UNII: YD01N1999R)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
ALLANTOIN (UNII: 344S277G0Z)
HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SODIUM OLEATE (UNII: 399SL044HN)
LAURETH-7 (UNII: Z95S6G8201)
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
STEARETH-2 (UNII: V56DFE46J5)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
ALCOHOL (UNII: 3K9958V90M)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
GERANIOL (UNII: L837108USY)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
BENZYL BENZOATE (UNII: N863NB338G)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
EUGENOL (UNII: 3T8H1794QW)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SORBIC ACID (UNII: X045WJ989B)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
CHLORPHENESIN (UNII: I670DAL4SZ)
METHYLPARABEN (UNII: A2I8C7HI9T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68026-503-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2017	12/31/2021
2	NDC: 68026-503-05	5 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2017	12/31/2021
3	NDC: 68026-503-01	1 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2017	12/31/2021
4	NDC: 68026-503-07	7 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2017	12/31/2021
5	NDC: 68026-503-15	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2017	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	10/22/2013	12/31/2021

Labeler - La Prairie, Inc. (606554996)