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

Is NDC 48783-0112-08 recalled?

Monsels Solution · 14 g in 1 VIAL, SINGLE-DOSE (48783-112-08)

Yes — this exact package was recalled

1 FDA recall names the code 48783-0112-08 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
Ferric Subsulfate
Strength
FERRIC SUBSULFATE 210 mg/g
Form
Paste · Topical
Labeler
Premier Dental Products Company
Type
Human Prescription Drug
Product code
48783-0112

Recalls naming this package

Class III · Low risk

Premier

Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the vial itself; the saleable unit of the box of 12 bottles has the correct expiration date printed.

Ongoing Labeling / mix-up Premier Dental Products Co NDC 48783-112-08 D-0490-2026

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.