NDC Code(s) : 31645-186-01, 31645-186-02
Packager : Physicians Formula Inc

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

City Glow Daily Defense BronzerTitanium Dioxide POWDER
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:31645-186
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 DIOXIDE15 g in 100 g
Inactive Ingredients
Ingredient Name Strength
TALC(UNII: 7SEV7J4R1U)
MICA(UNII: V8A1AW0880)
OCTYLDODECYL STEAROYL STEARATE(UNII: 3D47Q6D93C)
PROPANEDIOL(UNII: 5965N8W85T)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
CETYL DIMETHICONE 25(UNII: U4AS1BW4ZB)
SODIUM DEHYDROACETATE(UNII: 8W46YN971G)
BIS-DIGLYCERYL POLYACYLADIPATE-2(UNII: 6L246LAM9T)
WATER(UNII: 059QF0KO0R)
ZINC STEARATE(UNII: H92E6QA4FV)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:31645-186-021 in 1 CARTON 01/01/2015
1NDC:31645-186-0111 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 01/01/2015

PRINCIPAL DISPLAY PANEL

PDP