Quick answers
- What is Opcon-A?
- Opcon-A is a brand name of Naphazoline and pheniramine, an over-the-counter medicine. The FDA NDC Directory lists 2 Opcon-A products in 1 strength and form.
- Who makes Opcon-A?
- Bausch and Lomb holds the FDA application for Opcon-A (NDA020065, approved June 8, 1994).
- Is there a generic or store brand of Opcon-A?
- Yes. The FDA NDC Directory lists 5 other products with the same active ingredients, strength and form as a Opcon-A product. Ask your pharmacist whether one is right for you.
- Has Opcon-A been recalled?
- No recall linked to Opcon-A products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Opcon-A is
Each Opcon-A product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Naphazoline and pheniramine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| naphazoline hydrochloride 0.2675 mg/mL · pheniramine maleate 3.15 mg/mL solution/ drops (ophthalmic) | Opcon-A | 5 products, 5 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Naphazoline and pheniramine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020065 | Bausch and Lomb | June 8, 1994 | 2 |
Companies that list Opcon-A
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Opcon-A products.
- Bausch & Lomb Incorporated2 products
Recalls
No recall linked to Opcon-A products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.