Extralasting

Manufacturer
New Avon LLC | Avon Products, Inc.
Effective date
2016-02-17
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:45:15

Label at a glance#

ProductExtralasting Cream-to-Powder Foundation
Active ingredientOCTINOXATE, TITANIUM 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 ingredients

Octinoxate 6.34%...................................

Titanium Dioxide 3.00%............................

OTC - PURPOSE SECTION

                            Purpose
...................................Sunscreen
...................................Sunscreen

INDICATIONS & USAGE SECTION

Uses
• helps prevent sunburn

WARNINGS SECTION

WARNINGS
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
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

• limit time in the sun, especially from 10 a.m. – 2 p.m.

• wear long-sleeved shirts, pants, hats, and sunglasses

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients: Propylene Glycol Dicaprylate/Dicaprate, Diisopropyl Dimer Dilinoleate, Microcrystalline Wax/Cire Microcristalline, Nylon-12, Cetyl Ricinoleate, Hydrogenated Coco-Glycerides, Silica, Tribehenin, Punica Granatum Sterols, Polymethyl Methacrylate, Ethylene/Methacrylate Copolymer, Propylparaben, VP/Hexadecene Copolymer, Dimethicone, Ethylparaben, Triethoxycaprylylsilane, Glyceryl Rosinate, Octyldodecyl Myristate, Magnesium Myristate, Butylparaben, Tocopheryl Acetate, Isopropyl Titanium Triisostearate. 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 PDPimage of PDPimage of DFBimage of DFBimage of DFBimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0231-22020-01-31C16284748780-19d75b9d1-0e0a-f424-e053-dadaa90a57ce0f22a716-7eac-4933-bdc3-5ea5659f9ff3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0231-1ExtralastingCream-to-Powder Foundation9 g in 1 CASECREAM95
10096-0231-2ExtralastingCream-to-Powder Foundation1 in 1 CARTONCREAM15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0231EXTRALASTING CREAM-TO-POWDER FOUNDATION (OCTINOXATE, TITANIUM DIOXIDE) CREAM [NEW AVON LLC]5Legacy NDC, 2 package rows20160303_0f22a716-7eac-4933-bdc3-5ea5659f9ff3.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD514
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP4
OCTINOXATEACTIVE MOIETY4Y5P7MUD514
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP4

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-023110096-0231-1, 10096-0231-2

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
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
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
5b393da2-d964-4722-8e37-cf01d8b1e2290f22a716-7eac-4933-bdc3-5ea5659f9ff32016-02-17WarningsExact identifier
spl id: 5b393da2-d964-4722-8e37-cf01d8b1e229
spl set id: 0f22a716-7eac-4933-bdc3-5ea5659f9ff3

Reported adverse events (FAERS/openFDA)#

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