Skip to content
Lower risk Drug recall · FDA · Published March 20, 2017

Valeant CLENZIderm Acne Treatment Recall: Discoloration Risk

Valeant recalls 5 fl oz salicylic acid acne treatment due to potential discoloration. Learn if your product is affected and what to do.

🇺🇸 FDA recall #D-0672-2017DrugValeant ›
Take action

Contact the company

Recalling firmValeant Pharmaceuticals North America LLC400 Somerset Corporate Blvd · Bridgewater, NJ 08807-2867
✎ GovInfoNow plain-language explainer

What happened, in plain English

Valeant is recalling a specific acne treatment product because it may cause discoloration. This issue does not pose a health risk but could affect skin appearance. Read more at govinfonow.com/recall/41799-valeant-clenziderm-acne-treatment-recall-discoloration-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/41799-valeant-clenziderm-acne-treatment-recall-discoloration-risk · Updated October 8, 2026 · FDA enforcement record: FDA #D-0672-2017

Cite this page

“Valeant CLENZIderm Acne Treatment Recall: Discoloration Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41799-valeant-clenziderm-acne-treatment-recall-discoloration-risk. Based on FDA recall #D-0672-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0672-2017%22&limit=1).

Why it’s dangerous

The product may cause skin discoloration as a result of its salicylic acid content. This discoloration is not harmful but could be noticeable on the skin.

Who’s affected

People who own or use the recalled CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148 mL) product are affected. Those with sensitive skin may be at slightly higher risk of visible discoloration.

How to tell if you have this one

Check for the product name 'CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148 mL)' on the label. The product was distributed by OMP, Inc. in Long Beach, CA and made in the USA.

  • Brand
    Valeant
  • 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
Recall numberProduct, codes & lotsQuantity
D-0672-2017CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148 mL), Valeant Pharmaceuticals North America LLC Distributed by OMP, Inc Long Beach, CA 90806 Made in USA. Product SKU 301876102042, NDC 0187-6102-04; Lot #: 15J1277, Exp. 04/201738,767 units
D-0673-2017CLENZIderm M.D. Acne Treatment System, kit has 3 bottles a) Therapeutic Lotion (benzoyl peroxide 5% Acne Treatment) 47mL bottle, b) Daily Care Foaming Cleanser (Salicylic Acid 2% Acne Treatment) 118 mL bottle, c) Salicylic Acid 2% Acne Treatment 148mL, Valeant Pharmaceuticals North America LLC Distributed by OMP, Inc Long Beach, CA 90806 Made in USA, Product SKU 301876103018, NDC 0187-6103-01; Lot #: a) 15I1234, Exp. 09/18, b) 15E1221, Exp. 09/18, c) 15G1235 and 15I1236, Exp. 09/18.5,647 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name and SKU number 301876102042 on the label.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.2 years after the firm started it.

1. Firm started the recall: Mar 20, 201712. FDA classified it Class III: Apr 17, 201723. Published in FDA’s Enforcement Report: Apr 26, 201734. FDA terminated the recall: Jun 14, 2019420172019
  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.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

Yes, the product is safe for use but may cause discoloration in some users.

Similar recalls

Latest drug recalls

Keep exploring

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-0672-2017 (March 20, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0672-2017 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