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Actigraft

NAFDAC Reg. No. A3-101007 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 6 November 2026 · synced automatically from official sources.
Producto
Actigraft
Número NAFDAC
A3-101007
Principio activo
Wound Care Kit
Dosis
NA
Forma
NA
Tamaño del envase
1's
Fabricante
No Constan
Solicitante (titular)
Ies-Medical Ng Limited
Approved
29 Jul 2023
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
26 Jul 2028
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Wound care kit: uses, dosage and brands worldwide

Lo que encontramos

  • 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.

Generado automáticamente a partir del registro NAFDAC, QUIÉN alerta y los datos de la comunidad a partir de hoy. Este no es un consejo médico. Siga siempre a su médico o farmacéutico.

How to use Actigraft

Lo que dice el prospecto oficial. Si te lo recetó un médico, sigue la receta. Si el prospecto de tu caja es distinto, manda el de tu caja.

Para quién es

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

Posibles efectos secundarios

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.

Si olvidas una dosis

Tómala en cuanto te acuerdes, salvo que falte poco para la siguiente. En ese caso, sáltate la olvidada. Nunca tomes dos dosis a la vez para compensar. Revisa tu prospecto, porque algunos medicamentos son distintos.

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.

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy 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 6 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.