US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 13, 2020 (6 years ago)

Hydrocortisone butyrate Cream, 0.1%, 15-gram tubes, Rx Only, Manufactured for Oceanside…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

SUBPOTENT DRUG

What was recalled

Hydrocortisone butyrate Cream, 0.1%, 15-gram tubes, Rx Only, Manufactured for Oceanside Pharmaceuticals a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA, By: Ferndale Laboratories, Inc. Ferndale, MI 48220, NDC 68682-270-15

Recalling firm
Bausch Health Companies, Inc.
NDC code
68682-270-15
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0054-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Hydrocortisone recalls

See all