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ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device)

NAFDAC Reg. No. A3-100523 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device)
NAFDAC number
A3-100523
Active ingredient
Malaria Test
Strength
NA
Form
NA
Pack size
1 x 25's (in plastic bottle)
Manufacturer
Not listed
Applicant (holder)
Olpharm Nigeria Limited
Approved
2 Dec 2021
Status
Active View on NAFDAC ↗
Registration valid to
1 Dec 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) is on the NAFDAC register with an active registration (A3-100523). 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 ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) is used for

From the official U.S. FDA label for malaria test, the active ingredient registered with NAFDAC.

What it is used for

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to systemic or cutaneous infection from specific biological substances; including headache, nausea, abdominal pain, chills, occasional diarrhea, blurred vision, or food poisoning.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Purpose

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to systemic or cutaneous infection from specific biological substances; including headache, nausea, abdominal pain, chills, occasional …

Warnings

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

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

Check your pack of ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device)

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 ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device)

What is in ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device)?

ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) contains Malaria Test (NA), as na, according to its NAFDAC registration record.

Is ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) registered with NAFDAC?

Yes. ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) is listed on the NAFDAC register under registration number A3-100523, and its registration is active as of 27 October 2026.

Has ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) in our automatically synced alert list.

How can I check that my pack of ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) is genuine?

Run a free authenticity scan with the NAFDAC number A3-100523, 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 ParaHIT f Ver. 1.0 (Rapid Test for P.falciparum Malaria Device) used for?

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to systemic or cutaneous infection from specific biological substances; including headache, nausea, abdominal pain, chills, occasional diarrhea, blurred vision, or food poisoning.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. (Summarised from the official U.S. FDA label for malaria test. Always follow your doctor or pharmacist.)

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