NAFDAC Reg.-Nr. A4-8122 Medikament
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.
What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.
Temporarily relieves these symptoms due to hay fever or other respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat
Do not use if you ever had an allergic reaction to this product or any of its ingredients Ask a doctor before using if you have kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed do not take at the same time as aluminum or magnesium antacids do not take with fruit juices (see Directions) Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding, ask a healthcare professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away.
Keep out of reach of children.
Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.
Label for fexofenadine hydrochloride, the active ingredient registered with NAFDAC.
Add the expiry date on your pack for a full Trust Score.
Xonadine 120 mg contains Fexofenadine Hydrochloride (120 mg), as capsule, according to its NAFDAC registration record.
Yes. Xonadine 120 mg is listed on the NAFDAC register under registration number A4-8122, and its registration is active as of 6 November 2026.
No WHO falsified or substandard medical product alert currently matches Xonadine 120 mg in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A4-8122, 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: adults and children 12 years of age and over take one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hours children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor…
temporarily relieves these symptoms due to hay fever or other respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat (Summarised from the official U.S. FDA label for fexofenadine hydrochloride. 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.