SUPER CC PLUS CONCEALER SPF 30- titanium dioxide, zinc oxide cream
Physicians Formula Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Super CC Concealer-PF

active ingredients

warnings

inactive ingredients

pdp

SUPER CC PLUS CONCEALER SPF 30
titanium dioxide, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:31645-172
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	5.8 g in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	6 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
MICA (UNII: V8A1AW0880)
CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TEPRENONE (UNII: S8S8451A4O)
HYDROXYCAPRIC ACID (UNII: B41993WR8W)
HYDROXYCAPRYLIC ACID (UNII: 0R6X0G0S8A)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
APPLE FRUIT OIL (UNII: 9NT987I3A8)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:31645-172-02	1 in 1 CARTON	01/01/2014	12/31/2019
1	NDC:31645-172-01	4 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	01/01/2014	12/31/2019

Labeler - Physicians Formula Inc (021261805)

Registrant - Physicians Formula Inc (021261805)

Revised: 12/2019

Document Id: 9a04875a-800a-b3d4-e053-2995a90ab8a4

Set id: da1567fb-0c94-48c8-8243-1655a9c88886

Version: 4

Effective Time: 20191218

Physicians Formula Inc