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Drucedrin Capsules_

NAFDAC REG NO: A11-100969 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 6 November 2026 · synced automatically from official sources.
Produit
Drucedrin Capsules_
Numéro NAFDAC
A11-100969
Principe actif
Paracetamol; Diphenhydramine HCl
Dosage
500 mg; 25 mg
Forme
Capsule
Conditionnement
10 x 10's (in Alu PVC blisters)
Fabricant
Non répertorié
Déposant / Titulaire :
Drugfield Pharmaceuticals Limited
Approuvé
23 Sep 2025
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
23 Sep 2030
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Paracetamol: uses, dosage and brands worldwide

What we found

  • 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.

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 Drucedrin Capsules_

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

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

Comment le prendre et à quelle fréquence
  • 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. …

Effets secondaires possibles

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.

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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.

Ou prenez la boîte en photo
Encore 3 vérifications gratuites aujourd'hui 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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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.