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Vadilix Syrup_

NAFDAC Reg. No. 04-4113 · Drug

Registered with NAFDAC. Registration activeAs of 1 November 2026 · synced automatically from official sources.
Product
Vadilix Syrup_
رقم NAFDAC
04-4113
المادة الفعالة
Diphenhydramine HCl; Sodium citrate
التركيز
7 mg/5 mL; 28.5 mg/5 mL
الشكل
Syrup
حجم العبوة
1 x 100
Manufacturer
Not listed
Applicant (holder)
First Vadis Pharmaceutical Industries Limited
Approved
29 Oct 2025
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
28 Oct 2030
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

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

What we found

  • Vadilix Syrup_ is on the NAFDAC register with an active registration (04-4113). 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 Vadilix Syrup_

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

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

كيف يُتناول وكم مرة

• 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. …

الآثار الجانبية المحتملة

• 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.

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

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 Vadilix Syrup_

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

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم المصادر الرسمية: FDA الأمريكية · EMA (الاتحاد الأوروبي) · NAFDAC · تنبيهات منظمة الصحة العالمية

About Vadilix Syrup_

What is in Vadilix Syrup_?

Vadilix Syrup_ contains Diphenhydramine HCl; Sodium citrate (7 mg/5 mL; 28.5 mg/5 mL), as syrup, according to its NAFDAC registration record.

Is Vadilix Syrup_ registered with NAFDAC?

Yes. Vadilix Syrup_ is listed on the NAFDAC register under registration number 04-4113, and its registration is active as of 1 November 2026.

Has Vadilix Syrup_ been flagged as fake or recalled?

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

How can I check that my pack of Vadilix Syrup_ is genuine?

Run a free authenticity scan with the NAFDAC number 04-4113, 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 Vadilix 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 Vadilix 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.