eye itch relief

Generic: ketotifen fumarate

Labeler: target corporation
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name eye itch relief
Generic Name ketotifen fumarate
Labeler target corporation
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

ketotifen fumarate .25 mg/mL

Manufacturer
Target Corporation

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
histamine h1 receptor antagonists [moa] histamine-1 receptor inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673064
Hyphenated Format 11673-064

Supplemental Identifiers

RxCUI
311237
UNII
HBD503WORO

Packaging Origin

Original Packager
true

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
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • .25 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-064-05) / 5 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

ketotifen fumarate (.25 mg/mL)

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"}