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Panbio COVID-19 Ag Rapid Test Device (Nasal)

NAFDAC Reg. No. A3-100907 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Panbio COVID-19 Ag Rapid Test Device (Nasal)
NAFDAC number
A3-100907
Active ingredient
COVID-19 Test
Strength
NA
Form
NA
Pack size
1 x 25's (Tests in a box)
Manufacturer
Not listed
Applicant (holder)
Abbott Healthcare Nigeria Limited
Approved
24 Feb 2023
Status
Active View on NAFDAC ↗
Registration valid to
22 Feb 2028
WHO alerts
None found
Community reports
None
Times checked
0

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.

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

From the official U.S. FDA label for covid-, the active ingredient registered with NAFDAC.

What it is used for

Dilute with 5g of oil in 500ml of water

Purpose

Antibacterial, anti-fungal, indoor air purification, humidity control and insect repellent, sick house syndrome, formaldehyde neutralization, forest bathing effect and stress relief, sterilization deo …

Warnings

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

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

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

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

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 27 October 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.

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.