HIGH

Skin MD Body Acne Cleanser Recalled Due to Benzene Contamination

Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser on September 12, 2025. The recall follows the discovery of elevated benzene levels in the product. This contamination poses a high health risk to consumers in California and Georgia.

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 Skin MD Body Acne Cleanser, containing 10% benzoyl peroxide, in 7 oz (201 g) bottles. It is associated with Lot # 58170A and 58172A, with an expiration date of September 2025. The product was distributed in California and Georgia.

The Hazard

The recall was initiated due to the detection of elevated levels of benzene, a harmful chemical. Benzene exposure can lead to serious health issues, making this a significant safety concern.

Reported Incidents

No specific incidents or injuries have been reported related to this recall. However, the presence of benzene poses a high risk to users.

What to Do

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

Contact Information

For more information, visit the FDA website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0664-2025 or reach out to Private Label Skin Care Inc.

Key Facts

  • Recalled product: Skin MD Body Acne Cleanser
  • Contamination: Elevated benzene levels
  • Distribution: California and Georgia
  • Stop use immediately
  • Contact manufacturer for guidance
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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
Lot # 58172A
Affected States
CA, GA
Report Date
October 1, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE
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