Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 0363-0073-26 recalled?

Soothe

Yes — this exact package was recalled

1 FDA recall names the code 0363-0073-26 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
Bismuth subsalicylate
Strength
BISMUTH SUBSALICYLATE 525 mg/30mL
Form
Liquid · Oral
Labeler
Walgreens
Type
Human OTC Drug
Product code
0363-0073

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