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Accueil / Enregistré au Nigeria / Panbio COVID-19 Ag Rapid Test Device (Nasal)

Panbio COVID-19 Ag Rapid Test Device (Nasal)

NAFDAC REG NO: A3-100907 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 5 November 2026 · synced automatically from official sources.
Produit
Panbio COVID-19 Ag Rapid Test Device (Nasal)
Numéro NAFDAC
A3-100907
Principe actif
COVID-19 Test
Dosage
N/A
Forme
N/A
Conditionnement
1 x 25's (Tests in a box)
Fabricant
Non répertorié
Déposant / Titulaire :
Abbott Healthcare Nigeria Limited
Approuvé
24 Feb 2023
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
22 Feb 2028
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Covid-: uses, dosage and brands worldwide

What we found

  • Panbio COVID-19 Ag Rapid Test Device (Nasal) is on the NAFDAC register with an active registration (A3-100907). 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 Panbio COVID-19 Ag Rapid Test Device (Nasal)

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

Dilute with 5g of oil in 500ml of water

Comment le prendre et à quelle fréquence

for topical use only

Warnings

Do not drink. Beware of fire. Keep out of reach of children. Avoid direct sunlight. Do not use directly on the skin

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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 2020-08-01.

Label for covid-, the active ingredient registered with NAFDAC.

Check your pack of Panbio COVID-19 Ag Rapid Test Device (Nasal)

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

Ou prenez la boîte en photo
Encore 3 vérifications gratuites aujourd'hui Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Panbio COVID-19 Ag Rapid Test Device (Nasal)

What is in Panbio COVID-19 Ag Rapid Test Device (Nasal)?

Panbio COVID-19 Ag Rapid Test Device (Nasal) contains COVID-19 Test (NA), as na, according to its NAFDAC registration record.

Is Panbio COVID-19 Ag Rapid Test Device (Nasal) registered with NAFDAC?

Yes. Panbio COVID-19 Ag Rapid Test Device (Nasal) is listed on the NAFDAC register under registration number A3-100907, and its registration is active as of 5 November 2026.

Has Panbio COVID-19 Ag Rapid Test Device (Nasal) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Panbio COVID-19 Ag Rapid Test Device (Nasal) in our automatically synced alert list.

How can I check that my pack of Panbio COVID-19 Ag Rapid Test Device (Nasal) is genuine?

Run a free authenticity scan with the NAFDAC number A3-100907, 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 Panbio COVID-19 Ag Rapid Test Device (Nasal)?

Follow your prescription or the leaflet in your pack. The official label says: for topical use only…

What is Panbio COVID-19 Ag Rapid Test Device (Nasal) used for?

Dilute with 5g of oil in 500ml of water (Summarised from the official U.S. FDA label for covid-. 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.