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

Is NDC 0574-7093-12 recalled?

Hydrocortisone Acetate · 12 PACKET in 1 BOX (0574-7093-12) / 1 SUPPOSITORY in 1 PACKET

Yes — this exact package was recalled

1 FDA recall names the code 0574-7093-12 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
Hydrocortisone Acetate
Strength
HYDROCORTISONE ACETATE 30 mg/1
Form
Suppository · Rectal
Labeler
Padagis US LLC
Type
Human Prescription Drug
Product code
0574-7093

Recalls naming this package

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