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

Is NDC 46122-0741-38 recalled?

Magnesium Citrate · 296 mL in 1 BOTTLE, PLASTIC (46122-741-38)

Yes — this exact package was recalled

1 FDA recall names the code 46122-0741-38 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.

1 of these recalls is still ongoing.

Active ingredient
Magnesium Citrate
Strength
MAGNESIUM CITRATE 1.745 g/29.6mL
Form
Liquid · Oral
Labeler
Amerisource Bergen
Type
Human OTC Drug
Product code
46122-0741

Recalls naming this package

Class II ยท Moderate risk

Good Neighbor Pharmacy

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.

Ongoing Microbial contamination Pharma Nobis LLC NDC 46122-741-38 D-0227-2024

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