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Optalyn Eyedrops

NAFDAC Reg. No. A4-101324 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Optalyn Eyedrops
NAFDAC number
A4-101324
Active ingredient
Olopatadine (Olopatadine Hydrochloride)
Strength
0.2%
Form
Solution/Drops
Pack size
1 x 5 mL (in a container)
Manufacturer
Not listed
Applicant (holder)
Korlyns Pharmaceuticals Ltd
Approved
27 May 2025
Status
Active View on NAFDAC ↗
Registration valid to
26 May 2030
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Optalyn Eyedrops is on the NAFDAC register with an active registration (A4-101324). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What Optalyn Eyedrops is used for

From the official U.S. FDA label for olopatadine (olopatadine hydrochloride), the active ingredient registered with NAFDAC.

What it is used for

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

Purpose

Drug Facts Active Ingredients Purpose Olopatadine (0.1%) (equivalent to olopatadine hydrochloride 0.111%) Antihistamine and Redness Reliever

Possible side effects

you experience: eye pain changes in vision increased redness of the eye itching worsens or lasts for more than 72 hours

Do not use if

if solution changes color or becomes cloudy if you are sensitive to any ingredient in this product to treat contact lens related irritation When using this product do not touch tip of container to any surface to avoid contamination remove contact lenses before use wait at least 10 minutes before reinserting contact lenses after use do not wear a contact lens if your eye is red

Warnings

For external use only Do not use if solution changes color or becomes cloudy if you are sensitive to any ingredient in this product to treat contact lens related irritation When using this product do not touch tip of container to any surface to avoid contamination remove contact lenses before use wait at least 10 minutes before reinserting contact lenses after use do not wear a contact lens if your eye is red Stop use and ask a doctor if you experience: eye pain changes in vision increased redness of the eye itching worsens or lasts for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Storage

only for use in the eye store between 4°-25°C (39°-77°F)

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Optalyn Eyedrops

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Optalyn Eyedrops

What is in Optalyn Eyedrops?

Optalyn Eyedrops contains Olopatadine (Olopatadine Hydrochloride) (0.2%), as solution/drops, according to its NAFDAC registration record.

Is Optalyn Eyedrops registered with NAFDAC?

Yes. Optalyn Eyedrops is listed on the NAFDAC register under registration number A4-101324, and its registration is active as of 5 November 2026.

Has Optalyn Eyedrops been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Optalyn Eyedrops in our automatically synced alert list.

How can I check that my pack of Optalyn Eyedrops is genuine?

Run a free authenticity scan with the NAFDAC number A4-101324, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Optalyn Eyedrops used for?

temporarily relieves itchy and red eyes due to pollen, ragweed, grass, animal hair and dander (Summarised from the official U.S. FDA label for olopatadine (olopatadine hydrochloride). Always follow your doctor or pharmacist.)

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Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.