NDC Code(s) : 68026-801-30
Packager : La Prairie, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

La Prairie Skin Caviar Essence In Foundation SPF 25 Satin NudeAVOBENZONE, OCTINOXATE, OCTOCRYLENE EMULSION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68026-801
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVOBENZONE(UNII: G63QQF2NOX)
(AVOBENZONE - UNII:G63QQF2NOX) 		AVOBENZONE20 mg in 1 mL
OCTINOXATE(UNII: 4Y5P7MUD51)
(OCTINOXATE - UNII:4Y5P7MUD51) 		OCTINOXATE30 mg in 1 mL
OCTOCRYLENE(UNII: 5A68WGF6WM)
(OCTOCRYLENE - UNII:5A68WGF6WM) 		OCTOCRYLENE40 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
CYCLOMETHICONE 5(UNII: 0THT5PCI0R)
WATER(UNII: 059QF0KO0R)
GLYCERIN(UNII: PDC6A3C0OX)
ALKYL (C12-15) BENZOATE(UNII: A9EJ3J61HQ)
DIMETHICONE(UNII: 92RU3N3Y1O)
MYRISTYL LACTATE(UNII: 1D822OC34X)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER(UNII: WB5K9Y35Y9)
POLYGLYCERYL-4 ISOSTEARATE(UNII: 820DPX33S7)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LARICIFOMES OFFICINALIS FRUITING BODY(UNII: 7IFM8431X3)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)(UNII: UF7620L1W6)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S)(UNII: 1PEZ3NLY6I)
ASIAN GINSENG(UNII: CUQ3A77YXI)
EQUISETUM ARVENSE BRANCH(UNII: 1L0VKZ185E)
CAVIAR, UNSPECIFIED(UNII: 020K6HLU0O)
TETRAPEPTIDE-3(UNII: 90AX5T9G36)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
CHONDRUS CRISPUS CARRAGEENAN(UNII: UE856F2T78)
POLYOXYL 40 HYDROGENATED CASTOR OIL(UNII: 7YC686GQ8F)
LACTOBACILLUS REUTERI(UNII: 9913I24QEE)
.ALPHA.-TOCOPHEROL ACETATE(UNII: 9E8X80D2L0)
SOYBEAN OIL(UNII: 241ATL177A)
DISTEARDIMONIUM HECTORITE(UNII: X687XDK09L)
LACTIC ACID, UNSPECIFIED FORM(UNII: 33X04XA5AT)
ALUMINUM HYDROXIDE(UNII: 5QB0T2IUN0)
HYDROGENATED SOYBEAN LECITHIN(UNII: H1109Z9J4N)
EDETATE DISODIUM ANHYDROUS(UNII: 8NLQ36F6MM)
SODIUM LAUROYL GLUTAMATE(UNII: NCX1UU2D33)
PHYTATE SODIUM(UNII: 88496G1ERL)
TRIETHOXYCAPRYLYLSILANE(UNII: LDC331P08E)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)(UNII: 255PIF62MS)
LYSINE(UNII: K3Z4F929H6)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
SODIUM OLEATE(UNII: 399SL044HN)
SILICA DIMETHYL SILYLATE(UNII: EU2PSP0G0W)
ETHYLHEXYLGLYCERIN(UNII: 147D247K3P)
ALCOHOL(UNII: 3K9958V90M)
SACCHAROMYCES CEREVISIAE(UNII: 978D8U419H)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM SALICYLATE(UNII: WIQ1H85SYP)
SODIUM CHLORIDE(UNII: 451W47IQ8X)
BENZYL ALCOHOL(UNII: LKG8494WBH)
LINALOOL, (+/-)-(UNII: D81QY6I88E)
ISOMETHYL-.ALPHA.-IONONE(UNII: 9XP4LC555B)
GERANIOL(UNII: L837108USY)
.BETA.-CITRONELLOL, (R)-(UNII: P01OUT964K)
BENZYL SALICYLATE(UNII: WAO5MNK9TU)
SODIUM DEHYDROACETATE(UNII: 8W46YN971G)
SODIUM BENZOATE(UNII: OJ245FE5EU)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:68026-801-302 in 1 CARTON 15/05/2018
115 mL in 1 CONTAINER 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 05/15/2018

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