Label: EYE ITCH- ketotifen fumarate solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 30142-702-01 - Packager: Kroger Company
- 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:
COMPARE TO the active ingredient of
Zaditor® *See side panel
NDC 30142-702-01
Kroger Logo
ORIGINAL PRESCRIPTION STRENGTH
STERILE
Eye Itch
Relief Drops
Ketotifen Fumarate
Ophthalmic Solution 0.035%
Antihistamine Eye Drops
- Works in Minutes
- For Ages 3 Years
and Older - 30-Day Supply
LASTS UP TO
12HOURS
5 mL
(0.17 FL OZ)
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INGREDIENTS AND APPEARANCE
EYE ITCH
ketotifen fumarate solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-702 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:30142-702-01 1 in 1 CARTON 01/22/2014 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 01/22/2014 Labeler - Kroger Company (006999528) Registrant - Akorn Operating Company LLC (117693100) Establishment Name Address ID/FEI Business Operations Akorn 117696840 MANUFACTURE(30142-702) , ANALYSIS(30142-702) , STERILIZE(30142-702) , PACK(30142-702) , LABEL(30142-702) Establishment Name Address ID/FEI Business Operations Akorn AG 482198285 MANUFACTURE(30142-702) Establishment Name Address ID/FEI Business Operations Akorn 117696873 LABEL(30142-702) , PACK(30142-702)