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

Is NDC 66993-0877-61 recalled?

Calcipotriene · 1 TUBE in 1 CARTON (66993-877-61) / 60 g in 1 TUBE

Yes — this exact package was recalled

1 FDA recall names the code 66993-0877-61 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
Calcipotriene
Strength
CALCIPOTRIENE 50 ug/g
Form
Cream · Topical
Labeler
Prasco Laboratories
Type
Human Prescription Drug
Product code
66993-0877

Recalls naming this package

Class II ยท Moderate risk

Calcipotriene Cream 0.0005%

Incorrect/Undeclared excipients: inadvertent omission of a drug excipient from the the Authorized Generic label and also a warning regarding contact dermatitis from the brand product labeling not being incorporated into the Authorized Generic labeling.

Terminated Chemical / undeclared Leo Pharma INC NDC 66993-877-61 D-0510-2017

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