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Lower risk Drug recall · FDA · Published March 9, 2018

Alva-Amco Psoriasin Cream Recall: Subpotent Coal Tar Content

Alva-Amco recalls Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal due to coal tar content failing label claims. Product may not provide intended relief after 24 months.

🇺🇸 FDA recall #D-0589-2018DrugAlva-Amco ›
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Contact the company

Recalling firmAlva-Amco Pharmacal Companies., Inc.7711 N Merrimac Ave · Niles, IL 60714-3423
✎ GovInfoNow plain-language explainer

What happened, in plain English

Alva-Amco is recalling Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal because the coal tar content has degraded over time. This means the product may not work as advertised after its expiration date. Read more at govinfonow.com/recall/40780-alva-amco-psoriasin-cream-recall-subpotent-coal-tar-content.

Source Summary by GovInfoNow · govinfonow.com/recall/40780-alva-amco-psoriasin-cream-recall-subpotent-coal-tar-content · Updated October 7, 2026 · FDA enforcement record: FDA #D-0589-2018

Cite this page

“Alva-Amco Psoriasin Cream Recall: Subpotent Coal Tar Content.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40780-alva-amco-psoriasin-cream-recall-subpotent-coal-tar-content. Based on FDA recall #D-0589-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0589-2018%22&limit=1).

Why it’s dangerous

The product has failed to maintain its label claim of coal tar content over its 24-month shelf life. This means the cream may not provide the intended therapeutic benefits for conditions like psoriasis.

Who’s affected

People who own or use the recalled Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal (57g plastic tubes) are affected. Those with sensitive skin or severe psoriasis may be at slightly higher risk due to potential reduced effectiveness.

How to tell if you have this one

Check for the product name 'Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal' in 57g plastic tubes. Look for lot numbers 61031-63331 and expiration dates from April 2018 to November 2019.

  • Brand
    Alva-Amco
  • Product
    Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the product name, size (57g plastic tubes), and lot numbers listed in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA; Italy; Sweden; Germany; New Zealand; Netherlands; Australia; Moldova; United Kingdom; Mexico; Brazil; Chile; Greece; Spain; Norway; Belgium; Bulgaria” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

1. Firm started the recall: Mar 9, 201812. FDA classified it Class III: Mar 12, 201823. Published in FDA’s Enforcement Report: Mar 21, 201834. FDA terminated the recall: Jun 26, 2020420182020
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0589-2018 (March 9, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0589-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA