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

Is NDC 53329-0147-44 recalled?

Medline · 118 mL in 1 TUBE (53329-147-44)

Yes — this exact package was recalled

1 FDA recall names the code 53329-0147-44 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
miconazole nitrate
Strength
MICONAZOLE NITRATE 20 mg/mL
Form
Cream · Topical
Labeler
Medline Industries, LP
Type
Human OTC Drug
Product code
53329-0147

Recalls naming this package

Class II ยท Moderate risk

Medline Remedy Clinical TREAT Antifungal Cream

Labeling: Not Elsewhere Classified; Product labeling contains the claim of 'Paraben Free' while the product does in fact contain parabens as part of the formulation/ ingredient list.

Ongoing Labeling / mix-up MEDLINE INDUSTRIES, LP - Northfield D-0315-2024

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