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Início / Registado na Nigéria / Maxipol Paracetamol Suspension

Maxipol Paracetamol Suspension

NAFDAC Reg. No. A4-5668 · Drug

Registered with NAFDAC. Registration activeAs of 30 October 2026 · synced automatically from official sources.
Product
Maxipol Paracetamol Suspension
Número NAFDAC
A4-5668
Princípio ativo
Paracetamol
Dosagem
125 mg/5 mL
Forma
Suspension
Tamanho da embalagem
1 x 60 mL (in amber bottle)
Manufacturer
Not listed
Applicant (holder)
SKG - Pharma Ltd
Approved
28 Jan 2021
Situação
Inactive View on NAFDAC ↗
Registro válido até
27 Jan 2026
Alertas da OMS
None found
Community reports
None
Times checked
0
Commonly used to relieve mild to moderate pain and reduce fever. General information only — follow the dosage on the pack or your pharmacist's instructions.

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

What we found

  • Maxipol Paracetamol Suspension is on the NAFDAC register with an active registration (A4-5668). 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 Maxipol Paracetamol Suspension

O que diz a bula oficial. Se um médico receitou, siga a receita. Se a bula da sua caixa for diferente, vale a da sua caixa.

Para quem é

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

Como tomar e com que frequência
  • 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. …

Possíveis efeitos colaterais

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.

Se esquecer uma dose

Tome assim que lembrar, a menos que esteja quase na hora da próxima dose. Nesse caso, pule a dose esquecida. Nunca tome duas doses de uma vez para compensar. Confira a bula, pois alguns medicamentos são diferentes.

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, the active ingredient registered with NAFDAC.

Check your pack of Maxipol Paracetamol Suspension

Add the expiry date on your pack for a full Trust Score.

Ou tire fotos da caixa
Restam 3 verificações grátis hoje Fontes oficiais: FDA dos EUA · EMA (UE) · NAFDAC · alertas da OMS

About Maxipol Paracetamol Suspension

What is in Maxipol Paracetamol Suspension?

Maxipol Paracetamol Suspension contains Paracetamol (125 mg/5 mL), as suspension, according to its NAFDAC registration record.

Is Maxipol Paracetamol Suspension registered with NAFDAC?

Yes. Maxipol Paracetamol Suspension is listed on the NAFDAC register under registration number A4-5668, and its registration is active as of 30 October 2026.

Has Maxipol Paracetamol Suspension been flagged as fake or recalled?

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

How can I check that my pack of Maxipol Paracetamol Suspension is genuine?

Run a free authenticity scan with the NAFDAC number A4-5668, 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 Maxipol Paracetamol Suspension?

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 Maxipol Paracetamol Suspension 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. Always follow your doctor or pharmacist.)

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