NDC Code(s) : 71026-002-01, 71026-002-02, 71026-002-03, 71026-002-04
Packager : YADAH Co., Ltd.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

YADAH SILKY FIT CONCEALER BB POWER BRIGHTENINGOCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE CREAM
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71026-002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
(TITANIUM DIOXIDE - UNII:15FIX9V2JP) 		TITANIUM DIOXIDE89 mg in 1 mL
OCTINOXATE(UNII: 4Y5P7MUD51)
(OCTINOXATE - UNII:4Y5P7MUD51) 		OCTINOXATE75 mg in 1 mL
OCTISALATE(UNII: 4X49Y0596W)
(OCTISALATE - UNII:4X49Y0596W) 		OCTISALATE50 mg in 1 mL
ZINC OXIDE(UNII: SOI2LOH54Z)
(ZINC CATION - UNII:13S1S8SF37) 		ZINC CATION19.6 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
CYCLOMETHICONE 5(UNII: 0THT5PCI0R)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
PEG-10 DIMETHICONE (600 CST)(UNII: 8PR7V1SVM0)
CAPRYLYL TRISILOXANE(UNII: Q95M2P1KJL)
NIACINAMIDE(UNII: 25X51I8RD4)
GLYCERIN(UNII: PDC6A3C0OX)
MAGNESIUM SULFATE, UNSPECIFIED FORM(UNII: DE08037SAB)
TALC(UNII: 7SEV7J4R1U)
DISTEARDIMONIUM HECTORITE(UNII: X687XDK09L)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER(UNII: 9NH1UDD2RR)
CAPRYLYL GLYCOL(UNII: 00YIU5438U)
JOJOBA OIL(UNII: 724GKU717M)
.ALPHA.-TOCOPHEROL ACETATE(UNII: 9E8X80D2L0)
ARBUTIN(UNII: C5INA23HXF)
ALLANTOIN(UNII: 344S277G0Z)
CAPRYLHYDROXAMIC ACID(UNII: UPY805K99W)
ADENOSINE(UNII: K72T3FS567)
ASCORBYL TETRAISOPALMITATE(UNII: 47143LT58A)
ALOE VERA LEAF(UNII: ZY81Z83H0X)
OPUNTIA FICUS-INDICA(UNII: 23Z87HTQ6P)
MORUS ALBA BARK(UNII: 7O71A48NDP)
ZINC PIDOLATE(UNII: C32PQ86DH4)
ASCORBYL GLUCOSIDE(UNII: 2V52R0NHXW)
Stearic Acid(UNII: 4ELV7Z65AP)
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
FERRIC OXIDE RED(UNII: 1K09F3G675)
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:71026-002-021 in 1 CARTON 15/05/2017
1NDC:71026-002-0135 mL in 1 CONTAINER Type 0: Not a Combination Product
2NDC:71026-002-041 in 1 CARTON 15/05/2017
2NDC:71026-002-0310 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 05/15/2017

PRINCIPAL DISPLAY PANEL

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