NDC Code 24453-198-01 | pharmacompass.com

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

Flawless Tinted Moisturizer Light Octinoxate, Octisalate, Avobenzone LOTION

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE(UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g in 100 g
OCTISALATE(UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5.0 g in 100 g
AVOBENZONE(UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3.0 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
DIETHYLHEXYL CARBONATE(UNII: YCD50O0Z6L)
CASTOR OIL(UNII: D5340Y2I9G)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
ETHYL MACADAMIATE(UNII: ANA2NCS6V1)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5)(UNII: 035JKJ76MT)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
ISODODECANE(UNII: A8289P68Y2)
NEOPENTYL GLYCOL DIHEPTANOATE(UNII: 5LKW3C543X)
HYDROGENATED CASTOR OIL(UNII: ZF94AP8MEY)
MICROCRYSTALLINE WAX(UNII: XOF597Q3KY)
MAGNESIUM SULFATE, UNSPECIFIED(UNII: DE08037SAB)
SODIUM CHLORIDE(UNII: 451W47IQ8X)
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
HEXYL LAURATE(UNII: 4CG9F9W01Q)
POLYGLYCERYL-4 ISOSTEARATE(UNII: 820DPX33S7)
GLYCERYL DIBEHENATE(UNII: R8WTH25YS2)
SODIUM BENZOATE (UNII: OJ245FE5EU)
FERRIC OXIDE RED(UNII: 1K09F3G675)
TRIBEHENIN(UNII: 8OC9U7TQZ0)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
.ALPHA.-TOCOPHEROL ACETATE(UNII: 9E8X80D2L0)
MALTODEXTRIN(UNII: 7CVR7L4A2D)
ETHYLHEXYLGLYCERIN(UNII: 147D247K3P)
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
LYCIUM BARBARUM FRUIT(UNII: 930626MWDL)
SYRINGA VULGARIS WHOLE(UNII: U49SHU1VCI)
PALMITOYL TRIPEPTIDE-5(UNII: 2A3916MQHO)
ALTHAEA OFFICINALIS LEAF(UNII: E2QQV92338)
MELISSA OFFICINALIS (UNII: YF70189L0N)
BILBERRY(UNII: 9P2U39H18W)
GREEN TEA LEAF(UNII: W2ZU1RY8B0)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:24453-198-02	1 in 1 CARTON	06/01/2012
1	NDC:24453-198-01	48 g in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	06/01/2012

NDC 24453-198-01
API & Excipient Details