HIGH

Private Label Skin Care Recalls Benzoyl Peroxide Cleanser Over Benzene Risk

Private Label Skin Care recalled its Micronized BPO Gel Cleanser 10% on September 12, 2025. Elevated benzene levels prompted the recall in California and Georgia. Consumers must stop using the product immediately and seek guidance from healthcare providers.

Hazard Information

Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Private Label Skin Care Inc. or your healthcare provider for guidance. Notification method: Letter

Product Details

The recalled product is Micronized BPO Gel Cleanser 10% (Benzoyl Peroxide 10%), 7 oz (201 g). It was distributed in California and Georgia. The affected lot numbers are 58170A and 58172A with an expiration date of 09/2025.

The Hazard

This recall involves chemical contamination due to elevated levels of benzene. Benzene exposure can pose serious health risks including cancer.

Reported Incidents

No specific incidents have been reported at this time. The product's classification is Class II which indicates a moderate risk.

What to Do

Consumers should stop using the product immediately. Contact Private Label Skin Care Inc. or your healthcare provider for further guidance.

Contact Information

For more information, visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0667-2025.

Key Facts

  • Recalled product: Micronized BPO Gel Cleanser 10%
  • Recall initiated on September 12, 2025
  • Elevated benzene levels detected
  • Distributed in California and Georgia
  • Lot numbers: 58170A and 58172A
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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot # 58170A and 58172A
Exp Date: 09/2025
Affected States
CA, GA
Report Date
October 1, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE
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