equate Eye Itch Relief

Dosage form: solution
Ingredients: KETOTIFEN FUMARATE 0.25mg in 1mL
Labeler: Wal-Mart Stores Inc
NDC code: 49035-923

Wal-Mart Eye Itch Relief Drug Facts

Active ingredient

Ketotifen (0.025%)

(equivalent to ketotifen fumarate 0.035%)

Purpose

Antihistamine

Uses

Temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander.

Warnings

Do not use

if solution changes color or becomes cloudy
if you are sensitive to any ingredient in this product
to treat contact lens related irritation

When using this product

do not touch tip of container to any surface to avoid contamination
remove contact lenses before use
wait at least 10 minutes before reinserting contact lenses after use
replace cap after each use

Stop use and ask a doctor if

you experience any of the following:

eye pain
changes in vision
redness of the eye
itching worsens or lasts for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

Adults and children 3 years of age and older: Put 1 drop in the affected eye(s) twice daily, every 8-12 hours, no more than twice per day.
Children under 3 years of age: Consult a doctor.

Other information

only for use in the eye
store at 20-25°C (68-77 °F) [see USP Controlled Room Temperature]

Inactive ingredients

benzalkonium chloride 0.01%, glycerin, purified water. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).

Questions or comments?

1-888-287-1915

Package/Label Principal Display Panel

Compare to Zaditor® active ingredient

Eye Itch Relief

Ketotifen Fumarate Ophthalmic Solution

Antihistamine Eye Drops

Works in minutes

Original prescription strength

Up To 12 Hours

For ages 3 years and older

30 day supply

Sterile

30 Day Supply

Eye Itch Relief Carton Image 1

Eye Itch Relief Carton Image 2

EQUATE EYE ITCH RELIEF
ketotifen fumarate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-923
Route of Administration	OPHTHALMIC	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KETOTIFEN FUMARATE (KETOTIFEN)	KETOTIFEN	0.25 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN
WATER
HYDROCHLORIC ACID
SODIUM HYDROXIDE

Packaging
#	Item Code	Package Description
1	NDC:49035-923-01	1 BOTTLE (BOTTLE) in 1 CARTON
1		5 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA077958	07/08/2010

Labeler - Wal-Mart Stores Inc (051957769)

Revised: 06/2012

Document Id: 2f0771a2-88b7-4675-bdcb-98b93a094989

Set id: 37c5d7e3-73da-45e3-8165-cc8f0ed9d123

Version: 2

Effective Time: 20120605

Wal-Mart Stores Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

equate Eye Itch Relief

Further information

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Alli

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