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 neomycin, the active ingredient registered with NAFDAC.
First aid to help prevent infection in minor cuts, scrapes and burns
first aid antibiotic
if the condition persists or gets worse a rash or other allergic reaction develops.
in eyes over large areas of the body if you are allergic to any of the ingredients longer than 1 week unless directed by a doctor
For external use only.
Store at room temperature
Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.
Banedif Powder contains Neomycin; Bacitracin zinc (5 mg/g; 250 IU/g), as powder, according to its NAFDAC registration record.
Yes. Banedif Powder is listed on the NAFDAC register under registration number 04-1271, and its registration is active as of 6 November 2026.
No WHO falsified or substandard medical product alert currently matches Banedif Powder in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number 04-1271, 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.
First aid to help prevent infection in minor cuts, scrapes and burns (Summarised from the official U.S. FDA label for neomycin. 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.