Alcaftadine

Alcaftadine is an FDA drug label for the active ingredient ALCAFTADINE manufactured by Aurohealth LLC administered by OPHTHALMIC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230623.

Generic: ALCAFTADINE

Manufacturer: Aurohealth LLC

Product Type: HUMAN OTC DRUG

Route: OPHTHALMIC

Dosage Form:

NDC: 58602-605

Application: ANDA210659

Effective: 20230623

Active Ingredients: Drug Facts Active ingredient Alcaftadine 0.25%

Indications & Usage

Use temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander

Dosage & Administration

Directions adults and children 2 years of age and older: put 1 drop in the affected eye(s) once daily, if using other ophthalmic products while using this product, wait at least 5 minutes between each product replace cap after each use children under 2 years of age: consult a doctor

Contraindications

Not available.

Warnings

Warnings For external use only

Adverse Reactions