Magix

Manufacturer: Avon Products, Inc
Effective date: 2012-11-07
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:33:38

Label at a glance#

ProductMagix Face Perfector

Active ingredientOCTINOXATE, OCTISALATE

Label structure8 sections

Storage and handling

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

Contacts and useful links#

PhoneLabel contact1-800-FOR-AVON

PhoneLabel contact1-800-265-AVON

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Purpose

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

INDICATIONS & USAGE SECTION

Uses• helps prevent sunburn

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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

INACTIVE INGREDIENT SECTION

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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of DFBimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0158-2	2019-11-27	C162847	48780-1	9855d018-e081-cd31-e053-dbdaa90ab51a	b899725b-6df3-461d-90eb-fdf4e821b083

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-0158-1	MagixFace Perfector	30 mL in 1 TUBE	LOTION	30		2
10096-0158-2	MagixFace Perfector	1 in 1 CARTON	LOTION	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0158	MAGIX FACE PERFECTOR (OCTINOXATE, OCTISALATE) LOTION [AVON PRODUCTS, INC]	2	Legacy NDC, 2 package rows	20121113_b899725b-6df3-461d-90eb-fdf4e821b083.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	2
OCTISALATE	ACTIVE INGREDIENT	4X49Y0596W	2
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	2
OCTISALATE	ACTIVE MOIETY	4X49Y0596W	2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Magix Face Perfector
OCTINOXATE, OCTISALATE
OCTINOXATE
OCTISALATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0158	10096-0158-1, 10096-0158-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
OCTISALATE	4X49Y0596W	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
208d37f0-8214-4aa4-88cb-66d7d40d6350			b899725b-6df3-461d-90eb-fdf4e821b083	2012-11-07	Warnings	Exact identifier spl id: 208d37f0-8214-4aa4-88cb-66d7d40d6350 spl set id: b899725b-6df3-461d-90eb-fdf4e821b083

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.