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Inicio / Registrado en Nigeria / Drucedrin Capsules_

Drucedrin Capsules_

NAFDAC Reg. No. A11-100969 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 6 November 2026 · synced automatically from official sources.
Producto
Drucedrin Capsules_
Número NAFDAC
A11-100969
Principio activo
Paracetamol; Diphenhydramine HCl
Dosis
500 mg; 25 mg
Forma
Capsule
Tamaño del envase
10 x 10's (in Alu PVC blisters)
Fabricante
No Constan
Solicitante (titular)
Drugfield Pharmaceuticals Limited
Approved
23 Sep 2025
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
23 Sep 2030
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Paracetamol: uses, dosage and brands worldwide

Lo que encontramos

  • Drucedrin Capsules_ is on the NAFDAC register with an active registration (A11-100969). 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 Drucedrin Capsules_

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

Temporarily relieves minor aches and pains due to: headache the common cold backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever

Cómo tomarlo y con qué frecuencia
  • Do not take more than directed
  • Adults and children 12 years and over take 2 gelcaps every 6 hours while symptoms last
  • Do not take more than 6 gelcaps in 24 hours, unless directed by a doctor
  • Do not take for more than 10 days unless directed by a doctor
  • Children under 12 years: ask a doctor
Talk to a doctor first if

liver disease.

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If a skin reaction occurs, stop use and seek medical help right away. Do not use if you are allergic to acetaminophen or any of the inactive ingredients in this product with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. …

Posibles efectos secundarios

New symptoms occur pain gets worse or lasts more than 10 days fever gets worse or lasts more than 3 days redness or swelling is present These could be signs of a serious condition.

Pregnancy and breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

How to store it

Store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F) avoid high humidity see end flap for expiration date and lot number 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 2026-01-02.

Label for paracetamol and diphenhydramine hcl, the active ingredient registered with NAFDAC.

Check your pack of Drucedrin Capsules_

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 Drucedrin Capsules_

What is in Drucedrin Capsules_?

Drucedrin Capsules_ contains Paracetamol; Diphenhydramine HCl (500 mg; 25 mg), as capsule, according to its NAFDAC registration record.

Is Drucedrin Capsules_ registered with NAFDAC?

Yes. Drucedrin Capsules_ is listed on the NAFDAC register under registration number A11-100969, and its registration is active as of 6 November 2026.

Has Drucedrin Capsules_ been flagged as fake or recalled?

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

How can I check that my pack of Drucedrin Capsules_ is genuine?

Run a free authenticity scan with the NAFDAC number A11-100969, 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 Drucedrin Capsules_?

Follow your prescription or the leaflet in your pack. The official label says: do not take more than directed adults and children 12 years and over take 2 gelcaps every 6 hours while symptoms last do not take more than 6 gelcaps in 24 hours, unless directed by a doctor do not take for more than 10 days unless directed by a doctor children under 12 years: ask a doctor…

What is Drucedrin Capsules_ used for?

temporarily relieves minor aches and pains due to: headache the common cold backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever (Summarised from the official U.S. FDA label for paracetamol and diphenhydramine hcl. Always follow your doctor or pharmacist.)

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