Label: MAGIX FACE PERFECTOR- octinoxate, octisalate lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0158-1, 10096-0158-2 - Packager: Avon Products, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated November 7, 2012
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive ingredients:
Dimethicone, Cyclopentasiloxane, Calcium Sodium Borosilicate, Cellulose, Cetearyl Dimethicone Crosspolymer, Alumina, Acrylates/Dimethicone Copolymer, Silica, Nylon-12, HDI/Trimethylol Hexyllactone Crosspolymer, C30-45 Alkyl Methicone, C30-45 Olefin, PEG/PPG-20/23 Dimethicone, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Caprylyl Glycol, Dimethicone Crosspolymer, Polyethylene, Parfum/Fragrance, Boron Nitride.
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INGREDIENTS AND APPEARANCE
MAGIX FACE PERFECTOR
octinoxate, octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0158 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0158-2 1 in 1 CARTON 1 NDC:10096-0158-1 30 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/06/2012 Labeler - Avon Products, Inc (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc 005149471 manufacture(10096-0158)