![EXTRALASTING CREAM-TO-POWDER FOUNDATION (OCTINOXATE, TITANIUM DIOXIDE) CREAM [AVON PRODUCTS, INC.]](https://medic.hrt.org//dailymed/images/a27ca01d-38dd-4ede-81d9-f73e52a5e010/Extralasting CtoP DFB1.jpg)
![EXTRALASTING CREAM-TO-POWDER FOUNDATION (OCTINOXATE, TITANIUM DIOXIDE) CREAM [AVON PRODUCTS, INC.]](https://medic.hrt.org//dailymed/images/a27ca01d-38dd-4ede-81d9-f73e52a5e010/Extralasting CtoP DFB2.jpg)
![EXTRALASTING CREAM-TO-POWDER FOUNDATION (OCTINOXATE, TITANIUM DIOXIDE) CREAM [AVON PRODUCTS, INC.]](https://medic.hrt.org//dailymed/images/a27ca01d-38dd-4ede-81d9-f73e52a5e010/Extralasting CtoP PDP.jpg)
| NDC | 71110-0001-1, 71110-0001-2 |
| Set ID | a27ca01d-38dd-4ede-81d9-f73e52a5e010 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | Avon Products, Inc. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART352 |
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EXTRALASTING CREAM-TO-POWDER FOUNDATION
octinoxate, titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71110-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 63.4 mg in 1 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: O4446S9CRA) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) NYLON-12 (UNII: 446U8J075B) CETYL RICINOLEATE (UNII: 1P677500YD) HYDROGENATED COCO-GLYCERIDES (UNII: XDD37N2GPR) TRIBEHENIN (UNII: 8OC9U7TQZ0) PROPYLPARABEN (UNII: Z8IX2SC1OH) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLPARABEN (UNII: 14255EXE39) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) OCTYLDODECYL MYRISTATE (UNII: S013N99GR8) MAGNESIUM MYRISTATE (UNII: Z1917F0578) BUTYLPARABEN (UNII: 3QPI1U3FV8) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) MICA (UNII: V8A1AW0880) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71110-0001-2 1 in 1 CARTON 12/15/2010 1 NDC:71110-0001-1 9 g in 1 CASE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 12/15/2010 Labeler - Avon Products, Inc. (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 544863277 manufacture(71110-0001)
