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Homepage / Eingetragen in Nigeria / Opatanol Eye Drop 0.1% Solution

Opatanol Eye Drop 0.1% Solution

NAFDAC Reg.-Nr. A4-2926 Medikament

Registriert bei NAFDAC. Registrierung aktivAs of 6 November 2026 · synced automatically from official sources.
Produkt-
Opatanol Eye Drop 0.1% Solution
NAFDAC-Nummer
A4-2926
Wirkstoff
Olopatadine (Olopatadine Hydrochloride)
Stärke
0.1%
Form
Solution/Drops
Hersteller
Nicht aufgeführt
Applicant (holder)
Novartis Nigeria Limited
Approved
2 Dec 2021
Status
Active View on NAFDAC ↗
Registration valid to
1 Dec 2026
WER WARNT
None found
Community reports
None
Times checked
0

About the medicine: Olopatadine: uses, dosage and brands worldwide

What we found

  • Opatanol Eye Drop 0.1% Solution is on the NAFDAC register with an active registration (A4-2926). 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. This is not medical advice. Always follow your doctor or pharmacist.

How to use Opatanol Eye Drop 0.1% Solution

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

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

How to take it and how often
  • Adults and children 2 years of age and older: put 1 drop in the affected eye(s) twice daily, every 6 to 8 hours, no more than twice per day 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
Talk to a doctor first 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.

Possible side effects

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

How to store it

Only for use in the eye store between 4°-25°C (39°-77°F) Keep out of reach of children.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2024-03-25.

Label for olopatadine (olopatadine hydrochloride), the active ingredient registered with NAFDAC.

Check your pack of Opatanol Eye Drop 0.1% Solution

Add the expiry date on your pack for a full Trust Score.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Opatanol Eye Drop 0.1% Solution

What is in Opatanol Eye Drop 0.1% Solution?

Opatanol Eye Drop 0.1% Solution contains Olopatadine (Olopatadine Hydrochloride) (0.1%), as solution/drops, according to its NAFDAC registration record.

Is Opatanol Eye Drop 0.1% Solution registered with NAFDAC?

Yes. Opatanol Eye Drop 0.1% Solution is listed on the NAFDAC register under registration number A4-2926, and its registration is active as of 6 November 2026.

Has Opatanol Eye Drop 0.1% Solution been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Opatanol Eye Drop 0.1% Solution in our automatically synced alert list.

How can I check that my pack of Opatanol Eye Drop 0.1% Solution is genuine?

Run a free authenticity scan with the NAFDAC number A4-2926, 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.

How do I take Opatanol Eye Drop 0.1% Solution?

Follow your prescription or the leaflet in your pack. The official label says: adults and children 2 years of age and older: put 1 drop in the affected eye(s) twice daily, every 6 to 8 hours, no more than twice per day 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…

What is Opatanol Eye Drop 0.1% Solution 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 PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.