Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class III · Low risk Terminated Initiated Jul 6, 2020 (6 years ago)

Skin Medica Acne Treatment Lotion

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

What was recalled

Skin Medica Acne Treatment Lotion (Benzoyl Peroxide 2.5%), 2 Oz bottle, Distributed in the U.S.A. by Allergan, Irvine, CA 92612, NDC 0023-4965-02

Affected NDC 0023-4965-02

Compare with the code on your package — it is the most precise check available.

Recalling firm
Allergan PLC
NDC code
0023-4965-02
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1409-2020 · FDA notice

Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Allergan PLC

All 2020 recalls

Other wrong potency / content recalls from 2020

All wrong potency / content recalls
Class II · Moderate risk

Sensorcaine-MPF

Subpotent Drug: Low out-of-specification assay results for the epinephrine component.

Terminated Wrong potency / content Fresenius Kabi USA, LLC NDC 63323-462-01 D-0172-2021