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Homepage / Eingetragen in Nigeria / Banedif Powder

Banedif Powder

NAFDAC Reg.-Nr. 04-1271 Medikament

Registriert bei NAFDAC. Registrierung aktivAs of 1 November 2026 · synced automatically from official sources.
Produkt-
Banedif Powder
NAFDAC-Nummer
04-1271
Wirkstoff
Neomycin; Bacitracin zinc
Stärke
5 mg/g; 250 IU/g
Form
Powder
VPE:
5G
Hersteller
Nicht aufgeführt
Applicant (holder)
Afrab-Chem Limited
Approved
30 Jun 2026
Status
Inactive View on NAFDAC ↗
Registration valid to
29 Jun 2031
WER WARNT
None found
Community reports
None
Times checked
0

About the medicine: Neomycin: uses, dosage and brands worldwide

What we found

  • Banedif Powder is on the NAFDAC register with an active registration (04-1271). 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 Banedif Powder

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

First aid to help prevent infection in minor cuts, scrapes and burns

How to take it and how often

Clean the affected area Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily May be covered with a sterile bandage.

Talk to a doctor first if

deep or puncture wounds animal bites serious burns

Warnings

For external use only.

Possible side effects

If the condition persists or gets worse a rash or other allergic reaction develops.

How to store it

Store at room temperature Keep out of reach of children.

If you miss a dose

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.

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 2025-07-27.

Label for neomycin and bacitracin zinc, the active ingredient registered with NAFDAC.

Check your pack of Banedif Powder

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Banedif Powder

What is in Banedif Powder?

Banedif Powder contains Neomycin; Bacitracin zinc (5 mg/g; 250 IU/g), as powder, according to its NAFDAC registration record.

Is Banedif Powder registered with NAFDAC?

Yes. Banedif Powder is listed on the NAFDAC register under registration number 04-1271, and its registration is active as of 1 November 2026.

Has Banedif Powder been flagged as fake or recalled?

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

How can I check that my pack of Banedif Powder is genuine?

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.

How do I take Banedif Powder?

Follow your prescription or the leaflet in your pack. The official label says: Clean the affected area Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily May be covered with a sterile bandage.…

What is Banedif Powder used for?

First aid to help prevent infection in minor cuts, scrapes and burns (Summarised from the official U.S. FDA label for neomycin and bacitracin zinc. 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.