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Banedif Ointment## (strength format)

NAFDAC Reg. No. 04-2046 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Banedif Ointment## (strength format)
NAFDAC number
04-2046
Active ingredient
Zinc Bacitracin; Neomycin Sulphate; Zinc oxide
Strength
126.90mg; 181.69mg;11.71mg
Form
Ointment
Pack size
1 x 20 g (in plastic tube)
Manufacturer
Not listed
Applicant (holder)
Afrab-Chem Limited
Approved
30 Nov 2023
Status
Active View on NAFDAC ↗
Registration valid to
29 Nov 2028
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Banedif Ointment## (strength format) is on the NAFDAC register with an active registration (04-2046). 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.

What Banedif Ointment## (strength format) is used for

From the official U.S. FDA label for zinc bacitracin, the active ingredient registered with NAFDAC.

What it is used for

first aid to help prevent infection in: • minor cuts • scrapes • burns

Purpose

First aid antibiotic

Possible side effects

• you need to use longer than 1 week • condition persists or gets worse • rash or other allergic reaction develops

Do not use if

• in the eyes • over large areas of the body • if you are allergic to any of the ingredients

Warnings

For external use only Do not use • in the eyes • over large areas of the body • if you are allergic to any of the ingredients Ask a doctor before use if you have • deep or puncture wounds • animal bites • serious burns Stop use and ask a doctor if • you need to use longer than 1 week • condition persists or gets worse • rash or other allergic reaction develops Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Storage

• store at 20°-25°C (68°-77°F)

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Banedif Ointment## (strength format)

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Banedif Ointment## (strength format)

What is in Banedif Ointment## (strength format)?

Banedif Ointment## (strength format) contains Zinc Bacitracin; Neomycin Sulphate; Zinc oxide (126.90mg; 181.69mg;11.71mg), as ointment, according to its NAFDAC registration record.

Is Banedif Ointment## (strength format) registered with NAFDAC?

Yes. Banedif Ointment## (strength format) is listed on the NAFDAC register under registration number 04-2046, and its registration is active as of 27 October 2026.

Has Banedif Ointment## (strength format) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Banedif Ointment## (strength format) in our automatically synced alert list.

How can I check that my pack of Banedif Ointment## (strength format) is genuine?

Run a free authenticity scan with the NAFDAC number 04-2046, 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.

What is Banedif Ointment## (strength format) used for?

first aid to help prevent infection in: • minor cuts • scrapes • burns (Summarised from the official U.S. FDA label for zinc bacitracin. 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.