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Edge Antacid Suspension

NAFDAC Reg. No. A11-100688 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Edge Antacid Suspension
NAFDAC number
A11-100688
Active ingredient
Magnesium trisilicate; Light magnesium carbonate; Sodium bicarbonate; Aluminium magnesium silicate
Strength
250 mg/5 mL; 250 mg/5 mL; 250 mg/5 mL; 30 mg/5 mL
Form
Suspension
Pack size
200 mL (in amber colored BRUT bottle with transparent 10 mL measuring cup)
Manufacturer
Not listed
Applicant (holder)
Biopharma Nigeria Limited
Approved
30 Apr 2024
Status
Active View on NAFDAC ↗
Registration valid to
1 May 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Edge Antacid Suspension is on the NAFDAC register with an active registration (A11-100688). 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 Edge Antacid Suspension

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

place enough product on hadns to cover all surfaces. rub hands together until dry. supervise children uner 6 years of age when using this product to avoid swallowing.

How to take it and how often

for external use only

Warnings

irritation or rash occurs. Keep out of reach of children.

How to store it

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 2026-01-08.

Label for magnesium trisilicate and light magnesium carbonate and sodium bicarbonate and aluminium magnesium silicate, the active ingredient registered with NAFDAC.

Check your pack of Edge Antacid Suspension

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Edge Antacid Suspension

What is in Edge Antacid Suspension?

Edge Antacid Suspension contains Magnesium trisilicate; Light magnesium carbonate; Sodium bicarbonate; Aluminium magnesium silicate (250 mg/5 mL; 250 mg/5 mL; 250 mg/5 mL; 30 mg/5 mL), as suspension, according to its NAFDAC registration record.

Is Edge Antacid Suspension registered with NAFDAC?

Yes. Edge Antacid Suspension is listed on the NAFDAC register under registration number A11-100688, and its registration is active as of 28 October 2026.

Has Edge Antacid Suspension been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Edge Antacid Suspension in our automatically synced alert list.

How can I check that my pack of Edge Antacid Suspension is genuine?

Run a free authenticity scan with the NAFDAC number A11-100688, 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 Edge Antacid Suspension?

Follow your prescription or the leaflet in your pack. The official label says: for external use only…

What is Edge Antacid Suspension used for?

place enough product on hadns to cover all surfaces. rub hands together until dry. supervise children uner 6 years of age when using this product to avoid swallowing. (Summarised from the official U.S. FDA label for magnesium trisilicate and light magnesium carbonate and sodium bicarbonate and aluminium magnesium silicate. 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.