Label: EYE ITCH RELIEF- ketotifen fumarate solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-705-01 - Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 10, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
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
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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PRINCIPAL DISPLAY PANEL
Principal Display Panel Text for Carton Label:
CVS Health™ Logo Compare to the active
ingredient in Zaditor®*
NDC 59779-705-01
Eye Itch
Relief
KETOTIFEN FUMARATE
OPHTHALMIC SOLUTION 0.035%
Antihistamine eye drops
• Works in minutes
• Original prescription strength
• For ages 3 and older
• 30 day supply
GET UP TO
12
HOURS
OF RELIEF
Actual Product
Size on Side Panel
STERILE
5 mL (0.17 FL OZ)
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INGREDIENTS AND APPEARANCE
EYE ITCH RELIEF
ketotifen fumarate solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-705 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ketotifen fumarate (UNII: HBD503WORO) (Ketotifen - UNII:X49220T18G) Ketotifen 0.35 mg in 1 mL Inactive Ingredients Ingredient Name Strength benzalkonium chloride (UNII: F5UM2KM3W7) glycerin (UNII: PDC6A3C0OX) water (UNII: 059QF0KO0R) hydrochloric acid (UNII: QTT17582CB) sodium hydroxide (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-705-01 1 in 1 CARTON 02/07/2014 1 5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077958 02/07/2014 Labeler - CVS Pharmacy (062312574) Registrant - Akorn Operating Company LLC (117693100) Establishment Name Address ID/FEI Business Operations Akorn 117696840 MANUFACTURE(59779-705) , ANALYSIS(59779-705) , STERILIZE(59779-705) , PACK(59779-705) , LABEL(59779-705) Establishment Name Address ID/FEI Business Operations Akorn, AG 482198285 MANUFACTURE(59779-705) Establishment Name Address ID/FEI Business Operations Akorn 117696873 LABEL(59779-705) , PACK(59779-705)