Label: EYE ITCH RELIEF- ketotifen fumarate solution
- NDC Code(s): 70000-0522-1, 70000-0522-2
- Packager: Cardinal Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated December 8, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
- •
- if you are sensitive to any ingredient in this product
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- if solution changes color or becomes cloudy
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- to treat contact lens related irritation
When using this product
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- remove contact lenses before use
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- wait at least 10 minutes before re-inserting contact lenses after use
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- do not touch tip of container to any surface to avoid contamination
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- replace cap after each use
Stop use and ask a doctor if you experience any of the following:
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- eye pain
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- changes in vision
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- redness of the eyes
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- itching that worsens or lasts for more than 72 hours
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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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
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INGREDIENTS AND APPEARANCE
EYE ITCH RELIEF
ketotifen fumarate solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) 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:70000-0522-1 1 in 1 CARTON 08/07/2020 1 5 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:70000-0522-2 1 in 1 CARTON 08/07/2020 2 10 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 - Cardinal Health (063997360) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 079587625 MANUFACTURE(70000-0522) , PACK(70000-0522) , LABEL(70000-0522)