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Lower risk Drug recall · FDA · Published February 13, 2017

Perrigo Salicylic Acid Cream 6% Recall: Impurity Risk in Rx Products

Perrigo recalls 6% salicylic acid cream (400g) due to impurity issues in some batches. This may affect prescription products sold in the US. Consumers should check lot numbers on the label.

🇺🇸 FDA recall #D-0504-2017DrugPerrigo ›
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Contact the company

Recalling firmL. Perrigo Company515 Eastern Ave · Allegan, MI 49010-9070
✎ GovInfoNow plain-language explainer

What happened, in plain English

Perrigo is recalling prescription salicylic acid cream (6%, 400g bottles) because some batches contained impurities that failed quality tests. This could pose a health risk if the impurities interact with the body during use. Read more at govinfonow.com/recall/41957-perrigo-salicylic-acid-cream-6-recall-impurity-risk-in-rx.

Source Summary by GovInfoNow · govinfonow.com/recall/41957-perrigo-salicylic-acid-cream-6-recall-impurity-risk-in-rx · Updated October 8, 2026 · FDA enforcement record: FDA #D-0504-2017

Cite this page

“Perrigo Salicylic Acid Cream 6% Recall: Impurity Risk in Rx Products.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41957-perrigo-salicylic-acid-cream-6-recall-impurity-risk-in-rx. Based on FDA recall #D-0504-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0504-2017%22&limit=1).

Why it’s dangerous

The cream contained an organic impurity that didn't meet safety standards. This impurity could potentially cause health issues if the product is used as directed, though the risk is low and not immediately dangerous.

Who’s affected

Prescription users of salicylic acid cream (6%, 400g bottles) with lot numbers 098840 or 098779 from June 2018. People using the product for skin conditions like acne or psoriasis are most at risk.

How to tell if you have this one

Check the label for lot numbers 098840 or 098779 on the 400g salicylic acid cream (6%) bottle. The product is prescription-only and sold with NDC 45802-806-01.

  • Brand
    Perrigo
  • Product
    Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class III
  • Status
    Terminated
  • Distribution
    Nationwide within United States
Recall numberProduct, codes & lots
D-0503-2017Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC 45802-237-01, UPC 3 45802-237-01 9.; Lot #: 099534, Exp. 07/18; 099512 Exp. 06/18.
D-0504-2017Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, NDC 45802-806-01, UPC 3 45802-806-01 7.; Lot #: 098840, 098779, Exp.06/18.
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for lot numbers 098840 or 098779 on the 400g salicylic acid cream (6%) bottle.

Where it went and when

Where it was distributed

Distributed nationwide.

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 within United States” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Feb 13, 201712. FDA classified it Class III: Mar 1, 201723. Published in FDA’s Enforcement Report: Mar 8, 201734. FDA terminated the recall: Sep 26, 201742017
  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-0504-2017 (February 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0504-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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