NDC Code(s) : 61957-2613-1
Packager : Parfums Christian Dior

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

DIORSNOW Teint Fraicheur Eclaircissant White Reveal Fresh Transparency Liquid Foundation with Sunscreen Broad Spectrum SPF30 tints 010OCTINOXATE, TITANIUM DIOXIDE EMULSION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61957-2613
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OCTINOXATE(UNII: 4Y5P7MUD51)
(OCTINOXATE - UNII:4Y5P7MUD51) 		OCTINOXATE35 mg in 1 mL
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
(TITANIUM DIOXIDE - UNII:15FIX9V2JP) 		TITANIUM DIOXIDE40.2 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
METHYL TRIMETHICONE(UNII: S73ZQI0GXM)
ALCOHOL(UNII: 3K9958V90M)
DIMETHICONE(UNII: 92RU3N3Y1O)
PENTAERYTHRITYL TETRAETHYLHEXANOATE(UNII: XJ7052W897)
ALUMINUM HYDROXIDE(UNII: 5QB0T2IUN0)
MICA(UNII: V8A1AW0880)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
STEARIC ACID(UNII: 4ELV7Z65AP)
BETULA PUBESCENS RESIN(UNII: 9G931M6I4G)
SODIUM MYRISTOYL GLUTAMATE(UNII: AYU7QD893W)
DISTEARDIMONIUM HECTORITE(UNII: X687XDK09L)
PVP/VA COPOLYMER(UNII: D9C330MD8B)
SODIUM CITRATE(UNII: 1Q73Q2JULR)
GLYCERIN(UNII: PDC6A3C0OX)
PROPYLENE CARBONATE(UNII: 8D08K3S51E)
BUTYLATED HYDROXYTOLUENE(UNII: 1P9D0Z171K)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
DIAMOND(UNII: 6GRV67N0U2)
ECTOINE(UNII: 7GXZ3858RY)
BENZYL SALICYLATE(UNII: WAO5MNK9TU)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
CITRIC ACID MONOHYDRATE(UNII: 2968PHW8QP)
TOCOPHEROL(UNII: R0ZB2556P8)
SODIUM CHLORIDE(UNII: 451W47IQ8X)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)(UNII: 255PIF62MS)
PHAEODACTYLUM TRICORNUTUM(UNII: Y5W63E7HLV)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS(UNII: 22ADO53M6F)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
POTASSIUM PHOSPHATE, UNSPECIFIED FORM(UNII: B7862WZ632)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:61957-2613-11 in 1 CARTON 15/10/2016
130 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 10/15/2016 12/31/2018

PRINCIPAL DISPLAY PANEL

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