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

Is NDC 42291-0741-51 recalled?

Sodium Flouride · 1 TUBE in 1 CARTON (42291-741-51) / 53.2 mL in 1 TUBE

Yes — this exact package was recalled

1 FDA recall names the code 42291-0741-51 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
Sodium Fluoride
Strength
SODIUM FLUORIDE 5 mg/mL
Form
Paste, Dentifrice · Dental
Labeler
AvKARE
Type
Human Prescription Drug
Product code
42291-0741

Recalls naming this package

Class II · Moderate risk

Sodium Fluoride 1.1%

Cases of Sodium Fluoride 1.1% Prescription Dental Toothpaste may contain cartons labeled as Capsaicin Cream 0.025% but contain correctly labeled tubes of Sodium Fluoride 1.1% Prescription Dental Toothpaste

Terminated Labeling / mix-up Avkare LLC NDC 42291-741-51 D-1146-2023

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