Super CC Powder-PF-Cosm Grp

Super CC Plus Powder by

Drug Labeling and Warnings

Super CC Plus Powder by is a Otc medication manufactured, distributed, or labeled by Physicians Formula. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SUPER CC PLUS POWDER SPF 30- titanium dioxide, zinc oxide powder 
Physicians Formula

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 Powder-PF-Cosm Grp

Warnings:  For external use only.  Do not use on broken or damaged skin.

When using this product keep out of eyes.  Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children.  If product is swallowed, get medical help or contact a Poison Control Center right away.

Active Ingredients:  Titanium Dioxide 15%, Zinc Oxide 10%

Purpose: Sunscreen

SUPER CC PLUS POWDER  SPF 30
titanium dioxide, zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 31645-176
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	15 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MICA (UNII: V8A1AW0880)
BORON NITRIDE (UNII: 2U4T60A6YD)
ZINC STEARATE (UNII: H92E6QA4FV)
OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
DIMETHICONE (UNII: 92RU3N3Y1O)
CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
LAUROYL LYSINE (UNII: 113171Q70B)
TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYCAPRIC ACID (UNII: B41993WR8W)
HYDROXYCAPRYLIC ACID (UNII: 0R6X0G0S8A)
P-COUMARIC ACID (UNII: IBS9D1EU3J)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SALIX ALBA BARK VOLATILE OIL (UNII: PW3MX00JXN)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TEPRENONE (UNII: S8S8451A4O)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
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
1	NDC: 31645-176-02	1 in 1 CARTON	01/01/2014	01/01/2019
1	NDC: 31645-176-01	8.5 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	01/01/2014	01/01/2019

Labeler - Physicians Formula (021261805)

Registrant - Physicians Formula (021261805)

Revised: 12/2019

Document Id: 9a04509d-2973-fd96-e053-2995a90ad178

34390-5

Set id: 67528eb1-a3bd-40ab-8375-ffad07f941ca

Version: 3

Effective Time: 20191218

 

Physicians Formula