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Início / Registado na Nigéria / Zugokoff Cough Syrup

Zugokoff Cough Syrup

NAFDAC Reg. No. A11-101423 · Drug

Registered with NAFDAC. Registration activeAs of 15 November 2026 · synced automatically from official sources.
Product
Zugokoff Cough Syrup
Número NAFDAC
A11-101423
Princípio ativo
Diphenhydramine HCl; Sodium citrate
Dosagem
7 mg; 28.5 mg
Forma
Syrup
Tamanho da embalagem
1 x 100 mL (in amber PET bottle)
Manufacturer
Not listed
Applicant (holder)
ZUGOMED PHARMACEUTICALS LIMITED
Approved
27 Oct 2026
Situação
Active View on NAFDAC ↗
Registro válido até
26 Oct 2031
Alertas da OMS
None found
Community reports
None
Times checked
0

About the medicine: Sodium citrate: uses, dosage and brands worldwide

What we found

  • Zugokoff Cough Syrup is on the NAFDAC register with an active registration (A11-101423). 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 Zugokoff Cough Syrup

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

• for relief of occasional sleeplessness when associated with minor aches and pains • helps you fall asleep and stay asleep

Como tomar e com que frequência

• do not take more than directed • adults and children 12 years and over: take 2 caplets at bedtime • do not take more than 2 caplets in 24 hours

While you are taking it

• drowsiness will occur • avoid alcoholic drinks • do not drive a motor vehicle or operate machinery • take with food or milk if stomach upset occurs

Talk to a doctor first if

Ask a doctor before use if • stomach bleeding warning applies to you • you have problems or serious side effects from taking pain relievers or fever reducers • you have a history of stomach problems, such as heartburn • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke • you are taking a diuretic • you have a breathing problem such as emphysema or chronic bronchitis • you have glaucoma • you have trouble urinating due to an enlarged prostate gl …

Warnings

Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: • hives • facial swelling • asthma (wheezing) • shock • skin reddening • rash • blisters If an allergic reaction occurs, stop use and seek medical help right away. Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. …

Possíveis efeitos colaterais

• you experience any of the following signs of stomach bleeding: • feel faint • vomit blood • have bloody or black stools • have stomach pain that does not get better • you have symptoms of heart problems or stroke: • chest pain • trouble breathing • weakness in one part or side of body • slurred speech • leg swelling • pain gets worse or lasts more than 10 days • sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of a serious underlying medical illness. • redness or swelling is present in the painful area • any new symptoms appear

Pregnancy and breastfeeding

If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

How to store it

• read all warnings and directions before use. Keep carton. • store at 20-25°C (68-77°F) • avoid excessive heat above 40°C (104°F) 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 2025-04-21.

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

Check your pack of Zugokoff Cough Syrup

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

Ou tire fotos da caixa
Restam 3 verificações grátis hoje Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Zugokoff Cough Syrup

What is in Zugokoff Cough Syrup?

Zugokoff Cough Syrup contains Diphenhydramine HCl; Sodium citrate (7 mg; 28.5 mg), as syrup, according to its NAFDAC registration record.

Is Zugokoff Cough Syrup registered with NAFDAC?

Yes. Zugokoff Cough Syrup is listed on the NAFDAC register under registration number A11-101423, and its registration is active as of 15 November 2026.

Has Zugokoff Cough Syrup been flagged as fake or recalled?

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

How can I check that my pack of Zugokoff Cough Syrup is genuine?

Run a free authenticity scan with the NAFDAC number A11-101423, 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 Zugokoff Cough Syrup?

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 caplets at bedtime • do not take more than 2 caplets in 24 hours…

What is Zugokoff Cough Syrup used for?

• for relief of occasional sleeplessness when associated with minor aches and pains • helps you fall asleep and stay asleep (Summarised from the official U.S. FDA label for diphenhydramine hcl and sodium citrate. 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.