Gaviscon Antacid Recall: Missing Magnesium Warning Label
Gaviscon Regular Strength Liquid Antacid (12 oz) recalled for missing magnesium safety warning. Check your bottle label and lot numbers.
Lower-risk recall
Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.
Contact the company
What happened, in plain English
Glaxosmithkline Consumer Healthcare Holdings is recalling Gaviscon Regular Strength Liquid Antacid Cool Mint, 12 FL OZ bottles because the label lacks the required magnesium safety warning. The recall affects approximately 151,344 bottles distributed nationwide in the U.S.A. Consumers should check their product labels to see if they are affected. Read more at govinfonow.com/recall/37091-gaviscon-antacid-recall-missing-magnesium-warning-label.
Source Summary by GovInfoNow · govinfonow.com/recall/37091-gaviscon-antacid-recall-missing-magnesium-warning-label · Updated October 11, 2026 · FDA enforcement record: FDA #D-1323-2020
Cite this page
“Gaviscon Antacid Recall: Missing Magnesium Warning Label.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/37091-gaviscon-antacid-recall-missing-magnesium-warning-label. Based on FDA recall #D-1323-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1323-2020%22&limit=1).
Why it’s dangerous
The hazard is a labeling deficiency where the mandatory magnesium safety warning is absent from the bottle label. This means users may not be fully informed about specific safety information regarding magnesium content, though no physical defect in the product itself is described.
Who’s affected
Consumers in the U.S.A. who purchased Gaviscon Regular Strength Liquid Antacid Cool Mint, 12 FL OZ bottles between unspecified dates and still have them at home. Individuals relying on the magnesium warning for dosage or safety precautions are most impacted.
How to tell if you have this one
Check for Gaviscon Regular Strength Liquid Antacid Cool Mint, 12 FL OZ (355 mL) bottles distributed by GSK Consumer Healthcare Warren, NJ. Look for NDC 0135-0094-41 and lot numbers: 8H21C1 (Exp 7/31/2020), 9B25C1 (Exp 1/31/2021), 9D02C1 (Exp 2/28/2021), or 9G01C1 (Exp 5/31/2021). Verify that the label does not contain a magnesium safety warning.
- Brand
Gaviscon- Category
Drug
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
U.S.A. Nationwide
| Recall number | Product, codes & lots | Quantity | NDC |
|---|---|---|---|
| D-1322-2020 | Gaviscon Regular Strength Liquid Antacid Cool Mint, 6 FL OZ (177 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0094-42; Lot #: 8M17C1, Exp 11/30/2020; 9E30C1, Exp 4/30/2021; 9F05C1, Exp 4/30/2021 | 119,364 bottles | 0135-0094-41, 0135-0094-42, 0135-0095-41, 0135-0574-01 |
| D-1323-2020 | Gaviscon Regular Strength Liquid Antacid Cool Mint, 12 FL OZ (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0094-41; Lot #: 8H21C1, Exp 7/31/2020; 9B25C1, Exp 1/31/2021; 9D02C1, Exp 2/28/2021; 9G01C1, Exp 5/31/2021 | 151,344 bottles | 0135-0094-41, 0135-0094-42, 0135-0095-41, 0135-0574-01 |
| D-1324-2020 | Gaviscon Extra Strength Liquid Antacid Extra Strength Cherry, 12 FL OZ. (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0574-41; Lot #: 0A26C1, Exp 12/31/2021; 0B10C1, Exp 1/31/2022; 8L19C1, Exp 10/31/2020; 8L27C1, Exp 10/31/2020; 9A28C1, Exp 12/31/2020; 9B18C1, Exp 1/31/2021; 9C19C1, Exp 2/28/2021; 9D09C1, Exp 3/31/2021; 9F20C1, Exp 5/31/2021; 9G24C1, Exp 6/30/2021; 9J09C1, Exp 8/31/2021; 9K29C1, Exp 9/30/2021; 9L05C1, Exp 9/30/2021 | 629,796 bottles | — |
| D-1325-2020 | 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; Lot #: 0A21C1, Exp 12/31/2021; 0A31C1, Exp 12/31/2021; 0B05C1, Exp 12/31/2021; 8J04C1, Exp 7/31/2020; 8L05C1, Exp 9/30/200; 8L13C1 , Exp 10/31/2020; 9A14C1, Exp 12/31/2020; 9A21C1, Exp 12/31/2020; 9B04C1, Exp 12/31/2020; 9B11C1, Exp 1/31/2021; 9C04C1, Exp 1/31/2021; 9C12C1, Exp 2/28/2021; 9C25C1, Exp 2/28/2021; 9D17C1, Exp 3/312021; 9D24C1, Exp 3/312021; 9E01C1, Exp 3/31/2021; 9E10C1, Exp 3/31/2021; 9E21C1, Exp 4/30/2021; 9F11C1, Exp 5/31/2021; 9G15C1, Exp 6/30/2021; 9G30C1, Exp 6/30/2021; 9H06C1, Exp 6/30/2021; 9H12C1, Exp 7/31/2021, 9H2OC1, Exp 7/31/2021; 9H26C1, Exp 7/31/2021; 9J23C1, Exp 8/31/2021; 9J3OC1, Exp 8/31/2021; 9K08C1, Exp 8/31/2021; 9L11C1, Exp 10/31/2021; 9L18C1, Exp 10/31/2021; 9M02C1, Exp 10/31/2021; 9M09C1, Exp 11/30/2021; 9M17C1, Exp 11/30/2021; 19N1587221, Exp 7/31/2020; 19N1743754, Exp 12/31/2020; 19N1948440, Exp 6/30/2021; 19N1958219, Exp 6/30/2021; 20N2019997, Exp 7/31/2021; 20N2026258, Exp 8/31/2021; 20N2057778, Exp 8/31/2021 | 1,631,700 bottles & 27,300 Twin-Pack botles | 0135-0094-41, 0135-0094-42, 0135-0095-41, 0135-0574-01 |
What to do — step by step
Check Your Bottle Label
Inspect your Gaviscon bottle for NDC 0135-0094-41 and one of the specified lot numbers to see if it is part of this recall.
Verify Missing Warning
Confirm that the magnesium safety warning is missing from the label, as this is the specific defect triggering the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “U.S.A. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 20 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1323-2020 (May 28, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1323-2020 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.