FDA.reportPublic FDA data

Avon

Manufacturer
Avon Products, Inc.
Effective date
2011-04-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:27:50

Label at a glance#

ProductAvon Extralasting
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure6 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Uses: Helps prevent sunburn.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply evenly before sun exposure and as needed. Reapply
frequently for SPF benefit. Children under 6 months of age: Ask a health
care practitioner.

WARNINGS SECTION

WARNINGS: For external use only. When using this product, keep out of
eyes. If contact occurs, rinse thoroughly with water to remove. Stop use
and ask a health care practitioner if rash or irritation develops or lasts.
Keep out of reach of children. If swallowed, get medical help or contact a
Poison Control Center right away.

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: TITANIUM DIOXIDE 7.8%, ZINC OXIDE 6.86%.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS/INGRÉDIENTS INACTIFS: C12-15 ALKYL BENZOATE, NYLON-12,
TALC, LAUROYL LYSINE, SYNTHETIC FLUORPHLOGOPITE, ALUMINUM HYDROXIDE, DIMETHICONE,
ZINC STEARATE, CAPRYLYL GLYCOL, ISOBUTYLENE/STYRENE COPOLYMER, PPG-
12/SMDI COPOLYMER, KAOLIN, TRIETHOXYCAPRYLYLSILANE, CHITOSAN, METHICONE.
MAY CONTAIN/PEUT CONTENIR: MICA/CI 77019, TITANIUM DIOXIDE/CI 77891, IRON OXIDES.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of cartonimage of cartonimage of cartonimage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0260-22019-10-29C16284748780-1960f7f55-cf74-8e05-e053-dbdaa90a074a23f61a12-6721-4b09-8542-7ed04d65f9eb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0260-1AvonExtralasting12 g in 1 CASEPOWDER121
10096-0260-2AvonExtralasting1 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0260AVON EXTRALASTING (TITANIUM DIOXIDE, ZINC OXIDE) POWDER [AVON PRODUCTS, INC.]1Legacy NDC, 2 package rows20110428_23f61a12-6721-4b09-8542-7ed04d65f9eb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1

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
10096-026010096-0260-1, 10096-0260-2

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
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB

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
df80c035-9e6a-4179-a110-c7d996a4743b23f61a12-6721-4b09-8542-7ed04d65f9eb2011-04-22WarningsExact identifier
spl id: df80c035-9e6a-4179-a110-c7d996a4743b
spl set id: 23f61a12-6721-4b09-8542-7ed04d65f9eb

Reported adverse events (FAERS/openFDA)#

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