MAGIX FACE PERFECTOR- octinoxate and octisalate lotion 
Avon Products, 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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Active ingredients
Octinoxate 7.5%..................................................
Octisalate 4.0%...................................................

Purpose

..................................Sunscreen
..................................Sunscreen

Uses• helps prevent sunburn

Warnings
Skin Cancer/Skin Aging Alert:
Spending time in the sun increases your risk of skin cancer and early skin aging.This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

For external use only

Do not use on damaged or broken 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 swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply liberally 15 minutes before sun exposure

• children under 6 months of age: ask a doctor
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating

Other information
• protect the product in this container from excessive heat and direct sun


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.

Questions or Comments?
Call toll free 1-800-FOR-AVON or 1-800-265-AVON in Canada

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MAGIX  FACE PERFECTOR
octinoxate, octisalate lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0158
Route of Administration TOPICAL DEA Schedule     
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)

Revised: 11/2012
Document Id: 208d37f0-8214-4aa4-88cb-66d7d40d6350
Set id: b899725b-6df3-461d-90eb-fdf4e821b083
Version: 2
Effective Time: 20121107
 
Avon Products, Inc