NDC Code(s) : 31645-153-01, 31645-153-02
Packager : Physicians Formula Inc

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Mineral Wear Talc-Free Illuminating Powder Duo Titanium Dioxide, Zinc Oxide POWDER
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:31645-153
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 DIOXIDE12 g in 100 g
ZINC OXIDE(UNII: SOI2LOH54Z)
(ZINC OXIDE - UNII:SOI2LOH54Z) 		ZINC OXIDE4.2 g in 100 g
Inactive Ingredients
Ingredient Name Strength
LAUROYL LYSINE(UNII: 113171Q70B)
P-ANISIC ACID(UNII: 4SB6Y7DMM3)
MICA(UNII: V8A1AW0880)
BORON NITRIDE(UNII: 2U4T60A6YD)
ZINC STEARATE(UNII: H92E6QA4FV)
VITAMIN A PALMITATE(UNII: 1D1K0N0VVC)
.ALPHA.-TOCOPHEROL ACETATE, DL-(UNII: WR1WPI7EW8)
GLYCERYL CAPRYLATE(UNII: TM2TZD4G4A)
FERRIC OXIDE RED(UNII: 1K09F3G675)
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:31645-153-021 in 1 BOX 03/01/2010
1NDC:31645-153-0110 g 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 final part352 03/01/2010

PRINCIPAL DISPLAY PANEL

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