Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class III · Low risk Terminated Initiated Mar 9, 2018 (9 years ago)

Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal

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

Why it was recalled

Subpotent Drug: The product has failed to maintain its label claim of coal tar throughout its labeled 24-month expiry period.

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

Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed by: ALVA-AMCO Pharmacal Cos., Inc., Niles, IL 60714, USA. NDC 52389-745-56, UPC 0 72959 01045 4.

Affected NDC 52389-0745-56

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

Recalling firm
Alva-Amco Pharmacal Companies., Inc.
NDC code
52389-745-56
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0589-2018 · 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 wrong potency / content recalls from 2018

All wrong potency / content recalls
Class II · Moderate risk

Nitrofurantoin Oral Suspension

Subpotent Drug: Expansion of June 2018 recall of lots S700065 and S700619 due to below specification results for assay.

Terminated Wrong potency / content Lupin Somerset NDC 43386-450-11 D-0346-2019