RecallRadar

FDA Drug recall D-0026-2015

Locoid (hydrocortisone butyrate 0.1%), Cream, Net Wt. 15 gm tubes, Rx only, Manufactured for: Onset Dermatologics, LLC, Cumberland, RI 0286…

On 2014-10-22 the FDA classified a Class III recall of Locoid (hydrocortisone butyrate 0.1%), Cream, Net Wt. 15 gm tubes, Rx only, Manufactured for: Onset Dermatologics, LLC, Cumberland, RI 0286… by Valeant Pharmaceuticals International, citing subpotent Drug; for the active, HCB, and preservatives, Propylparaben and Butylparaben at the 18 month stability test point.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0026-2015
ClassificationClass III
Statusterminated
Initiated2014-10-02
Published2014-10-22
Last updated2026-09-13 11:51 UTC
CompanyValeant Pharmaceuticals International
DistributionUS

Product

Locoid (hydrocortisone butyrate 0.1%), Cream, Net Wt. 15 gm tubes, Rx only, Manufactured for: Onset Dermatologics, LLC, Cumberland, RI 02864 By: Ferndale Laboratories, Inc. Ferndale, MI 48220 --- NDC 16781-382-15

Reason

Subpotent Drug; for the active, HCB, and preservatives, Propylparaben and Butylparaben at the 18 month stability test point

Identifiers

code_infoLot number 13052B, Exp. 03/2015, NDC16781-382-15

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0026-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.