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Actigraft

NAFDAC Reg. Rárá. A3-101007 · Oògùn

Forukọsilẹ pẹlu NAFDAC. Iforukọsilẹ ti nṣiṣe lọwọAs of 5 November 2026 · synced automatically from official sources.
Ọja
Actigraft
Nọmba NAFDAC
A3-101007
Ohun elo ti nṣiṣe lọwọ
Wound Care Kit
Agbara
NA
Fọọmu
NA
Iwọn iṣakojọpọ
1's
Olupese
Ko ṣe atokọ
Olubẹwẹ (oluranlowo)
Ies-Medical Ng Limited
Ti fọwọsi
29 Jul 2023
Ipò
Nṣiṣẹ Wo lórí NAFDAC ↗
Iforukọsilẹ wulo si
26 Jul 2028
Tani o ṣe itaniji
Kosi ikankan ti a rii.
Ijabọ Agbegbe
Kò sí
Àwọn àyẹ̀wò àsìkò
0

Nipa oogun naa: Wound care kit: uses, dosage and brands worldwide

What we found

  • Actigraft is on the NAFDAC register with an active registration (A3-101007). 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 Actigraft

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

Tani o jẹ fun

Wash with mild skin cleanser. Pat dry or allow to air dry. Apply an ample amount of ointment over affected skin. Cover with a clean bandage. Repeat procedure every 12 hours until skin improves or as directed by a doctor.

Talk to a doctor first if

Consulting a doctor before using on deep or puncture wounds, animal bites or serious burns.

Warnings

For external use only, When using this product do not get into eyes

Àbájáde tí ó ṣeéṣe

Your condition worsens, does not improve, persists for more than 7 days, or occurs again after a few days.

How to store it

Store at room temperature. may stain fabrics 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 2026-02-13.

Label for wound care kit, the active ingredient registered with NAFDAC.

Check your pack of Actigraft

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 Actigraft

What is in Actigraft?

Actigraft contains Wound Care Kit (NA), as na, according to its NAFDAC registration record.

Is Actigraft registered with NAFDAC?

Yes. Actigraft is listed on the NAFDAC register under registration number A3-101007, and its registration is active as of 5 November 2026.

Has Actigraft been flagged as fake or recalled?

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

How can I check that my pack of Actigraft is genuine?

Run a free authenticity scan with the NAFDAC number A3-101007, 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 Actigraft used for?

Wash with mild skin cleanser. Pat dry or allow to air dry. Apply an ample amount of ointment over affected skin. Cover with a clean bandage. Repeat procedure every 12 hours until skin improves or as directed by a doctor. (Summarised from the official U.S. FDA label for wound care kit. 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.