Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 53943-0107-07 recalled?

Multi Symptom Antacid

Yes — this exact package was recalled

1 FDA recall names the code 53943-0107-07 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
Calcium carbonate ,Magnesium hydroxide,Simethicone
Strength
CALCIUM CARBONATE 675 mg/1; MAGNESIUM HYDROXIDE 135 mg/1…
Form
Tablet, Chewable · Oral
Labeler
Discount Drug Mart
Type
Human OTC Drug
Product code
53943-0107

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