KETOTIFEN FUMARATE- ketotifen fumarate solution 
CVS Pharmacy


Drug Facts

Active ingredient

Ketotifen (0.025%)

(equivalent to ketotifen fumarate 0.035%)




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


For external use only

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.


Other information

Inactive ingredients

benzalkonium chloride 0.01%, glycerol, hydrochloric acid and/or sodium hydroxide, and water for injection

Questions or comments?

Write to:

Apotex Corp.

Consumer Affairs

2400 N. Commerce Pkwy,

Suite 400,

Weston FL 33326

or call us at 1-800-706-5575 (Monday to Friday 8:30 am – 5:00 pm Eastern Standard Time)

Principal Display Panel - Bottle Label

CVS Pharmacy

NDC 69842-600-01

Ketotifen Fumarate Opthalmic Solution 0.025% 5 ml bottle


Principal Display Panel - Bottle Carton

CVS Pharmacy

NDC 69842-600-01

Ketotifen Fumarate Opthalmic Solution 0.025% 5 ml bottle


ketotifen fumarate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-600
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Ketotifen Fumarate (UNII: HBD503WORO) (Ketotifen - UNII:X49220T18G) Ketotifen 0.25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Glycerin (UNII: PDC6A3C0OX)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Hydrochloric Acid (UNII: QTT17582CB)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-600-011 in 1 CARTON06/01/2018
15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:69842-600-022 in 1 CARTON06/01/2018
25 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Labeler - CVS Pharmacy (062312574)
Registrant - Apotex Inc (209429182)
NameAddressID/FEIBusiness Operations
Apotex Inc255092496analysis(69842-600) , manufacture(69842-600)
NameAddressID/FEIBusiness Operations
Sifavitor SPA437723684api manufacture(69842-600)

Revised: 6/2018
Document Id: 080c7a34-c57a-12d1-61cc-f58873896373
Set id: 3cd76a82-1cdb-d701-cf95-ef5b6ad1fc4c
Version: 1
Effective Time: 20180601
CVS Pharmacy