Label: EYE ITCH RELIEF- ketotifen fumarate solution
- NDC Code(s): 67296-2245-5
- Packager: Redpharm Drug
- This is a repackaged label.
- Source NDC Code(s): 70000-0522
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated May 27, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
Do not use
- if you are sensitive to any ingredient in this product
- if solution changes color or becomes cloudy
- to treat contact lens related irritation
When using this product
- remove contact lenses before use
- wait at least 10 minutes before re-inserting contact lenses after use
- do not touch tip of container to any surface to avoid contamination
- replace cap after each use
Stop use and ask a doctor ifyou experience any of the following:
- eye pain
- changes in vision
- redness of the eyes
- itching that worsens or lasts for more than 72 hours
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Package/Label Principal Display Panel
LEADER[heart icon]™
NDC 70000-0522-2
Sterile / Eye Drops
Eye Itch
Relief
ketotifen fumarate
ophthalmic solution 0.035%
ANTIHISTAMINE EYE DROPSUp to 12 Hours
Works in Minutes
Original Prescription Strength
For Ages 3 Years and Older
COMPARE to
Systane ZADITOR
active ingredient*100% Money
Back Guarantee0.34 FL OZ (10 mL)9688902
F860109
-
INGREDIENTS AND APPEARANCE
EYE ITCH RELIEF
ketotifen fumarate solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67296-2245(NDC:70000-0522) Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KETOTIFEN FUMARATE (UNII: HBD503WORO) (KETOTIFEN - UNII:X49220T18G) KETOTIFEN 0.25 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) GLYCERIN (UNII: PDC6A3C0OX) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67296-2245-5 1 in 1 CARTON 08/07/2020 1 5 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021996 08/07/2020 Labeler - Redpharm Drug (828374897) Establishment Name Address ID/FEI Business Operations Redpharm Drug 828374897 repack(67296-2245)

