NAFDAC Reg. No. A4-100388 · Drug
About the medicine: Dextromethorphan hydrobromide: uses, dosage and brands worldwide
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.
ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.
Temporarily: ■ relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants ■ helps reduce the intensity of coughing
Label
Do Not Use ■ if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have ■ persistent or chronic cough such as occurs with smoking, asthma, or emphysema ■ cough that occurs with too much phlegm (mucus) Stop use and ask a doctor if cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious condition. …
Keep out of reach of children.
تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.
Label for dextromethorphan hydrobromide, the active ingredient registered with NAFDAC.
Add the expiry date on your pack for a full Trust Score.
Vixa Night-Time Softgel Capsules contains Dextromethorphan Hydrobromide (10 mg), as capsule, according to its NAFDAC registration record.
Yes. Vixa Night-Time Softgel Capsules is listed on the NAFDAC register under registration number A4-100388, and its registration is active as of 12 November 2026.
No WHO falsified or substandard medical product alert currently matches Vixa Night-Time Softgel Capsules in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A4-100388, 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.
Follow your prescription or the leaflet in your pack. The official label says: Label…
temporarily: ■ relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants ■ helps reduce the intensity of coughing (Summarised from the official U.S. FDA label for dextromethorphan hydrobromide. Always follow your doctor or pharmacist.)
Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.