magix

Manufacturer
Avon Products, Inc
Effective date
2009-12-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:33:44

Label at a glance#

Productmagix Cashmere Finish Liquid Foundation
Active ingredientTITANIUM DIOXIDE
Label structure8 sections

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active/Medicinal Ingredient
Titanium Dioxide 3.39% W/W...............................

OTC - PURPOSE SECTION

Purpose
.....................................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/non-medicinal ingredients: Cyclopentasiloxane, Water/Eau,Dimethicone, Glycerin, Dimethicone Crosspolymer, Polysilicone-11, Dimethicone/PEG-10/15 Crosspolymer, Petrolatum, Hydrolyzed Silk, Phenoxyethanol, Sodium Chloride, Caprylyl Glycol, Triethoxycaprylylsilane, Talc, Disodium EDTA, Aluminum Dimyristate, Disodium Stearoyl Glutamate, Dipropylene Glycol, Laureth-12, Methicone, Parfum/Fragrance, Tocopherol, Alumina, Cellulose, Silica, Cetearyl Dimethicone Crosspolymer, PEG/PPG-20/23 Dimethicone. May Contain: Titanium Dioxide/CI 77891, Iron Oxides, Mica/CI 77019, Bismuth Oxychloride/CI 77163.

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 labelimage of DFBimage of DFBimage of DFBimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0189-22019-11-27C16284748780-19855d018-d5b6-cd31-e053-dbdaa90ab51ae1212f19-d7cc-40a7-a0a8-5a686b2e949e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0189-1magixCashmere Finish Liquid Foundation30 mL in 1 TUBELOTION304
10096-0189-2magixCashmere Finish Liquid Foundation1 in 1 CARTONLOTION14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0189MAGIX CASHMERE FINISH LIQUID FOUNDATION (TITANIUM DIOXIDE) LOTION [AVON PRODUCTS, INC]4Legacy NDC, 2 package rows20121116_e1212f19-d7cc-40a7-a0a8-5a686b2e949e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP4
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP4

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-018910096-0189-1, 10096-0189-2

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
acb0ee1d-4140-4c73-bba8-0a0dde0e587be1212f19-d7cc-40a7-a0a8-5a686b2e949e2009-12-29WarningsExact identifier
spl id: acb0ee1d-4140-4c73-bba8-0a0dde0e587b
spl set id: e1212f19-d7cc-40a7-a0a8-5a686b2e949e

Reported adverse events (FAERS/openFDA)#

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