mark got the goods

Manufacturer
New Avon LLC | Avon Products, Inc.
Effective date
2016-02-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:45:18

Label at a glance#

Productmark got the goods multi-benefit foundation
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, OXYBENZONE
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 7.49%.........
Titanium Dioxide 2.6%...
Oxybenzone 2.0%.........

OTC - PURPOSE SECTION

     Purpose
..... Sunscreen

..... 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: Water/Eau, Butylene Glycol, Ethylhexyl Palmitate, Cyclopentasiloxane, Cetyl PEG/PPG-10/1 Dimethicone, Glyceryl
Stearate, PEG-40 Stearate, Silica, Steareth-2, Stearic Acid, Euphorbia Cerifera (Candelilla) Wax/Cire De Candelilla, Dimethicone, PEG-10
Dimethicone, Magnesium Aluminum Silicate, Triethanolamine, Glycerin, Imidazolidinyl Urea, Methylparaben, Alumina, Methicone, Xanthan Gum, Hydrolyzed Elastin, Ethylparaben, Kaolin, Punica Granatum Fruit Juice, Saccharomyces Lysate Extract, Sodium Hexametaphosphate, Tetrasodium EDTA, Zinc PCA, Phenyl Trimethicone, Beeswax/Cire D'abeille, Yeast Extract/Extrait De Levure, Salix Nigra (Willow) Bark Extract, Tocopheryl Acetate, Retinyl Palmitate, Sodium PCA, Olea Europaea (Olive) Leaf Extract, Urea, Silica Dimethyl Silylate, Hyaluronic Acid, Trehalose, Polyquaternium-51, Sodium Hyaluronate, Daucus Carota Sativa (Carrot) Root Extract, Tocopherol, Atelocollagen, Sodium Chondroitin Sulfate. May Contain: Iron Oxides, Titanium Dioxide/CI 77891, Mica/CI 77019.

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

PDPPDPDFBDFBDFBDFBDFBDFBDFBDFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0281-22020-01-31C16284748780-19d75b9d0-31b7-f424-e053-dadaa90a57cedc756ca2-9a84-4778-bdbc-8da0d92eff30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0281-1mark got the goodsmulti-benefit foundation30 mL in 1 BOTTLE, PUMPLOTION303
10096-0281-2mark got the goodsmulti-benefit foundation1 in 1 CARTONLOTION13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0281MARK GOT THE GOODS MULTI-BENEFIT FOUNDATION (OCTINOXATE, TITANIUM DIOXIDE, OXYBENZONE) LOTION [NEW AVON LLC]3Legacy NDC, 2 package rows20160303_dc756ca2-9a84-4778-bdbc-8da0d92eff30.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y2
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
OXYBENZONEACTIVE MOIETY95OOS7VE0Y2
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP2

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-028110096-0281-1, 10096-0281-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
OXYBENZONE95OOS7VE0YACTIB

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
aec97a2d-6d9b-43fd-9548-0d54d488985bdc756ca2-9a84-4778-bdbc-8da0d92eff302016-02-17WarningsExact identifier
spl id: aec97a2d-6d9b-43fd-9548-0d54d488985b
spl set id: dc756ca2-9a84-4778-bdbc-8da0d92eff30

Reported adverse events (FAERS/openFDA)#

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