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

Is NDC 55910-0183-38 recalled?

citroma · 296 mL in 1 BOTTLE, PLASTIC (55910-183-38)

Yes — this exact package was recalled

1 FDA recall names the code 55910-0183-38 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.

Active ingredient
Magnesium Citrate
Strength
MAGNESIUM CITRATE 1.745 g/29.6mL
Form
Liquid · Oral
Labeler
Old East Main Co.
Type
Human OTC Drug
Product code
55910-0183

Recalls naming this package

Class I ยท High risk

Rexall

Microbial contamination of non-sterile products.

Terminated Microbial contamination Vi-Jon, LLC NDC 55910-183-38 D-1506-2022

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