Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.
From the official U.S. FDA label for Durex Fetherlite Xl, the active ingredient registered with NAFDAC.
Temporarily relieves: pain & burning • frequency and urgency of urination
Antibacterial Analgesic (pain reliever)
Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. If changes in behaviour with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness. Stomach bleeding warning: This product contains an NSAID, which may cause stomach bleeding. …
• each tablet contains 25 mg of sodium • store at 59-86°F (15-30°C) in a dry place • protect from light • Tamper evident: tablets sealed in blisters. Do not use if blister foil or seal is open or damaged.
Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.
Durex Fetherlite Xl contains Condoms (NA), as na, according to its NAFDAC registration record.
Yes. Durex Fetherlite Xl is listed on the NAFDAC register under registration number A3-100583, and its registration is active as of 5 November 2026.
No WHO falsified or substandard medical product alert currently matches Durex Fetherlite Xl in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A3-100583, 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.
Temporarily relieves: pain & burning • frequency and urgency of urination (Summarised from the official U.S. FDA label for Durex Fetherlite Xl. Always follow your doctor or pharmacist.)
Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.