Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Gaviscon Liquid Antacid Extra Strength Recalled by Glaxosmithkline Consumer Healthcare Holdings Due to Labeling: Label lacks warning - Magnesium safety warning...

Date: May 28, 2020
Company: Glaxosmithkline Consumer Healthcare Holdings
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Glaxosmithkline Consumer Healthcare Holdings directly.

Affected Products

Gaviscon Liquid Antacid Extra Strength, Cool Mint, 12 FL OZ (355 mL) single pack and twin pack, Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0095-41

Quantity: 1,631,700 bottles & 27,300 Twin-Pack botles

Why Was This Recalled?

Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Glaxosmithkline Consumer Healthcare Holdings

Glaxosmithkline Consumer Healthcare Holdings has 16 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report