mark. get a tint

Manufacturer: Avon Products, Inc.
Effective date: 2012-05-23
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:32:09

Label at a glance#

Productmark. get a tint tinted moisturizer

Active ingredientOCTINOXATE, TITANIUM DIOXIDE

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 5.99%.........
Titanium Dioxide 5.81%...

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:

     WATER/EAU
     BUTYLENE GLYCOL
     CYCLOPENTASILOXANE
     PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE
     POLYSORBATE 60
     OCTYLDODECYL NEOPENTANOATE
     GLYCOL STEARATE
     PPG-2 MYRISTYL ETHER PROPIONATE
     CYCLOHEXASILOXANE
     SORBITAN STEARATE
     GLYCERIN
     NYLON-12
     SILICA
     ALUMINUM HYDROXIDE
     STEARIC ACID
     MAGNESIUM ALUMINUM SILICATE
     XANTHAN GUM
     SODIUM HEXAMETAPHOSPHATE
     DIMETHICONE
     ETHYLENE/ACRYLIC ACID COPOLYMER
     SODIUM HYALURONATE
     TOCOPHERYL ACETATE
     TETRASODIUM EDTA
     PHENOXYETHANOL
     METHYLPARABEN
MAY CONTAIN:
       TITANIUM DIOXIDE/CI 77891
       IRON OXIDES
       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

labelDFBDFBDFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0173-2	2019-11-13	C162847	48780-1	97449f38-c05f-f6ea-e053-dbdaa90aa703	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-0173-1	mark. get a tinttinted moisturizer	50 mL in 1 TUBE	LOTION	50		2
10096-0173-2	mark. get a tinttinted moisturizer	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
10096-0173	MARK. GET A TINT TINTED MOISTURIZER (OCTINOXATE, TITANIUM DIOXIDE) LOTION [AVON PRODUCTS, INC.]	2	Legacy NDC, 2 package rows	20120531_d367d566-5ff6-4d55-a903-559f70ec7436.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	2
TITANIUM DIOXIDE	ACTIVE INGREDIENT	15FIX9V2JP	2
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	2
TITANIUM DIOXIDE	ACTIVE MOIETY	15FIX9V2JP	2

Products#

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

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

mark. get a tint tinted moisturizer
Octinoxate, Titanium Dioxide
OCTINOXATE
TITANIUM DIOXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0173	10096-0173-1, 10096-0173-2

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
TITANIUM DIOXIDE	15FIX9V2JP	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
9a4aa372-2642-4132-9024-4cdb368fe869			d367d566-5ff6-4d55-a903-559f70ec7436	2012-05-23	Warnings	Exact identifier spl id: 9a4aa372-2642-4132-9024-4cdb368fe869 spl set id: d367d566-5ff6-4d55-a903-559f70ec7436

Reported adverse events (FAERS/openFDA)#

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