Skip to content
Drug recall · FDA · Published January 11, 2019

Oxalis Labs recalls Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: Macleods Pharma USA, Inc.

Oxalis Labs recalls 0.05% Clobetasol Propionate Topical Solution bottles due to leakage complaints. Affected units have specific lot numbers and expiration dates. Consumers should check their product details.

🇺🇸 FDA recall #D-0492-2019DrugOxalis Labs ›
Take action

Contact the company & request your remedy

Recalling firmOxalis LabsLodhimajra, Tehsil - Baddi · Theda, N/A N/A
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Oxalis Labs is recalling 50mL Clobetasol Propionate Topical Solution bottles because they have leaked. This could lead to product contamination or skin irritation if the solution comes into contact with skin. Read more at govinfonow.com/recall/39248-oxalis-labs-clobetasol-topical-solution-recall-leakage-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/39248-oxalis-labs-clobetasol-topical-solution-recall-leakage-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0492-2019

Cite this page

“Oxalis Labs Clobetasol Topical Solution Recall: Leakage Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39248-oxalis-labs-clobetasol-topical-solution-recall-leakage-risk. Based on FDA recall #D-0492-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0492-2019%22&limit=1).

Why it’s dangerous

The containers have leaked in the past, which could cause the solution to come into contact with skin. This might lead to skin irritation or contamination if the product is not properly handled.

Who’s affected

People who own or use the recalled Clobetasol Propionate Topical Solution 0.05% w/w, 50mL bottles. Those with sensitive skin may be at higher risk of irritation.

How to tell if you have this one

Check for the product name 'Clobetasol Propionate Topical Solution USP 0.05% w/w, 50 mL' on the bottle. Look for lot numbers PCA801A through PCA807A with expiration dates 12/2019 or 04/2020.

  • Brand
    Oxalis Labs
  • Product
    Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: Macleods Pharma USA, Inc.
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Identify the product name, lot numbers, and expiration dates to confirm if your bottle is affected.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall is due to leakage complaints, but the product is generally safe if the container is intact. Affected units should be checked for leaks.

How do I know if my product is recalled?

Check for lot numbers PCA801A through PCA807A with expiration dates 12/2019 or 04/2020 on the bottle label.

What should I do if I have the recalled product?

The recall does not specify a remedy, so check with Oxalis Labs for further instructions if you have the affected product.

Take action

Contact Oxalis Labs

We’ve drafted a message you can send Oxalis Labs to request your refund or repair — edit it as you like.

Subject: Recall D-0492-2019 — Oxalis Labs Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: 

Hello,

I own a Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: Macleods Pharma USA, Inc. that is covered by recall D-0492-2019 from Oxalis Labs.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

Keep exploring

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Comments are reviewed before they appear. No links, ads, or personal attacks — those get removed.

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-0492-2019 (January 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0492-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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