eye itch relief
Generic: ketotifen fumarate
Labeler: target corporationDrug Facts
Product Profile
Brand Name
eye itch relief
Generic Name
ketotifen fumarate
Labeler
target corporation
Dosage Form
SOLUTION
Routes
Active Ingredients
ketotifen fumarate .25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
11673-064
Product ID
11673-064_316940f0-2e63-f04f-e063-6394a90ae1a3
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA021996
Listing Expiration
2026-12-31
Marketing Start
2014-01-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673064
Hyphenated Format
11673-064
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
eye itch relief (source: ndc)
Generic Name
ketotifen fumarate (source: ndc)
Application Number
NDA021996 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .25 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (11673-064-05) / 5 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "316940f0-2e63-f04f-e063-6394a90ae1a3", "openfda": {"unii": ["HBD503WORO"], "rxcui": ["311237"], "spl_set_id": ["b25106f8-436e-4c06-8780-b12368ede9fe"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-064-05) / 5 mL in 1 BOTTLE", "package_ndc": "11673-064-05", "marketing_start_date": "20140102"}], "brand_name": "Eye Itch Relief", "product_id": "11673-064_316940f0-2e63-f04f-e063-6394a90ae1a3", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Inhibitor [EPC]"], "product_ndc": "11673-064", "generic_name": "ketotifen fumarate", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eye Itch Relief", "active_ingredients": [{"name": "KETOTIFEN FUMARATE", "strength": ".25 mg/mL"}], "application_number": "NDA021996", "marketing_category": "NDA", "marketing_start_date": "20140102", "listing_expiration_date": "20261231"}