CLASS III Drug recall · Reported 3 Apr 2013 · FDA Enforcement Report

Derma-Smoothe/FS (fluocinolone acetonide) recalled

Hill Dermaceuticals is recalling Derma-Smoothe/FS (fluocinolone acetonide), 0.01% Topical Oil (Body Oil), distributed nationwide in the US. The recall was initiated on 21 Nov 2012 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot J111040, Exp. (09/13)
Quantity recalled8,736 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-217-2013
FDA event ID
64455
Recalling firm
Hill Dermaceuticals, Sanford, FL
Classification
Class III
Status
Terminated
Recall initiated
21 Nov 2012
FDA classified
22 Mar 2013
Reported
3 Apr 2013
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Potency & Assay

Timeline

21 Nov 2012Recall initiated by company
22 Mar 2013Classified by FDA+121 days
3 Apr 2013Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent; 12 month stability timepoint

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Derma-Smoothe/FS (fluocinolone acetonide), 0.01% Topical Oil (Body Oil), Rx only, Hill Dermaceuticals, Inc., Sanford, Florida 32773 --- NDC 28105-150-04

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Subpotent; 12 month stability timepoint

Which lots are affected?

Lot J111040, Exp. (09/13)

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 64455

This product is part of a recall event; the main page for the event is Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIIDerma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical recalledHill DermaceuticalsPotency & AssayNationwide

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