Same formulation, different label. Identical to Opcon-A® and Naphcon-A®. Choose on price and availability, not on the drug.
Approved uses
Allergic conjunctivitis, itching and redness
1 or 2 drops in the affected eye(s) up to 4 times daily, age 6 years and over
Cuts redness more than either component alone, and beats olopatadine 0.1% at 12 and 20 minutes post-challenge.
Contraindications
Sensitivity to naphazoline, pheniramine, or any component of the product.
Available Forms
Ophthalmic solution, 15 mL (0.5 fl oz) dropper bottle, 15 mL twin pack
Mechanism of Action
Mixed alpha-1/alpha-2 adrenergic agonist (naphazoline) that constricts conjunctival vessels, combined with a first generation H1 antagonist (pheniramine) that blocks histamine-mediated itch. Decongestants with alpha-1 activity are associated with tachyphylaxis and rebound redness on repeated use, unlike the alpha-2 selective agonist brimonidine 0.025%.
Warnings & Precautions
Rebound hyperemia: Chronic use can produce conjunctivitis medicamentosa; in a 70 patient case series of naphazoline, tetrahydrozoline or phenylephrine users, patterns were conjunctival hyperemia (50 cases), follicular conjunctivitis (17), and eczematoid blepharoconjunctivitis (3), with a median 4 weeks to resolution after discontinuation.
Narrow angle glaucoma: Label-listed precaution; the product transiently enlarges the pupil.
Cardiovascular and prostatic disease: Caution in cardiac disease, hypertension, and benign prostatic hyperplasia with urinary difficulty.
Oral ingestion in children: Accidental oral ingestion in infants and children may lead to coma and marked reduction in body temperature.
Persistent symptoms: Eye pain, vision change, or redness or irritation that worsens or lasts more than 72 hours warrants examination rather than continued use.
Common Side Effects
Ocular: Temporary pupil enlargement, brief tingling on instillation, and increased redness with overuse; no frequencies given.
Systemic: Not characterized in this OTC label.
Pregnancy & Lactation
No adequate and well-controlled studies in pregnant women. It is not known whether this drug is excreted in human milk
Pediatric Use
Labeled for age 6 years and over; under 6, the label directs consultation.