MAGIX FACE PERFECTOR- octinoxate, octisalate lotion

Magix by

Drug Labeling and Warnings

Magix by is a Otc medication manufactured, distributed, or labeled by Avon Products, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients
Octinoxate 7.5%..................................................
Octisalate 4.0%...................................................

Purpose

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

INDICATIONS & USAGE

Uses helps prevent sunburn

WARNINGS

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.

DOSAGE & ADMINISTRATION

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

STORAGE AND HANDLING

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

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.

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MAGIX  FACE PERFECTOR
octinoxate, octisalate lotion

Product 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)