Class II · Moderate risk
Gaviscon Liquid Antacid Extra Strength
Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.
National Drug Code
Is NDC 0135-0095-41 recalled?
Gaviscon · 355 mL in 1 BOTTLE (0135-0095-41)
Yes — this exact package was recalled
1 FDA recall names the code 0135-0095-41 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- aluminum hydroxide and magnesium carbonate
- Strength
- ALUMINUM HYDROXIDE 254 mg/5mL; MAGNESIUM CARBONATE 237.5…
- Form
- Liquid · Oral
- Labeler
- Haleon US Holdings LLC
- Type
- Human OTC Drug
- Product code
- 0135-0095
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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