MARK. GET DEFENSIVE SPF 15 EYE- octinoxate, oxybenzone, octisalate, avobenzone cream

mark. by

Drug Labeling and Warnings

mark. by is a Otc medication manufactured, distributed, or labeled by Avon Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

USES: HELPS PREVENT SUNBURN. HIGHER SPF GIVES MORE SUNBURN PROTECTION.

DOSAGE & ADMINISTRATION

DIRECTIONS: APPLY IN THE MORNING. PAT ON EYELIDS AND UNDER EYES. APPLY EVENLY BEFORE SUN EXPOSURE AND AS NEEDED. REAPPLY AS NEEDED OR AFTER TOWEL DRYING, SWIMMING, OR PERSPIRING. CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR.

WARNINGS

WARNINGS: FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT, KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE. STOP USE AND ASK A DOCTOR IF RASH OR IRRITATION DEVELOPS AND LASTS. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:
     OCTINOXATE 7.5%    
     OXYBENZONE 3.0%
     OCTISALATE 3.0%
     AVOBENZONE 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:

     WATER/EAU
     GLYCERIN
     DIMETHICONE
     SILICA
     ARISTOTELIA CHILENSIS FRUIT JUICE
     GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT
     MEDICAGO SATIVA (ALFALFA) EXTRACT
     CARBOMER
     BENZYL ALCOHOL
     PEG-40 STEARATE
     STEARETH-2
     GLYCERYL STEARATE
     HYDROGENATED POLYDECENE
     PENTYLENE GLYCOL
     DIMETHICONE CROSSPOLYMER
     METHYLPARABEN
     SODIUM HYDROXIDE
     TETRASODIUM EDTA
     RIBES NIGRUM (BLACK CURRANT) BUD WAX
     CITRUS AURANTIUM DULCIS (ORANGE) FLOWER WATER
     PROPYLPARABEN
     ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
     ASCORBYL PALMITATE
     PHYTOL
     RETINYL PALMITATE
     GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER
     SODIUM HYALURONATE
     PHOSPHORIC ACID
     TOCOPHEROL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MARK.  GET DEFENSIVE SPF 15 EYE
octinoxate, oxybenzone, octisalate, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0255
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.125 mL  in 15 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	0.45 mL  in 15 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.45 mL  in 15 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.3 mL  in 15 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0255-2	1 in 1 CARTON
1	NDC: 10096-0255-1	15 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/14/2011

Labeler - Avon Products, Inc. (001468693)

Establishment
Name	Address	ID/FEI	Business Operations
Avon Products, Inc.		005149471	manufacture