HIGH

Private Label Skin Care Recalls Acne Treatment Over Benzene Contamination

Private Label Skin Care recalled its 7 oz Acne Treatment on September 12, 2025. Elevated levels of benzene prompted the recall, classified as Class II. The affected product was distributed in California and Georgia only.

Quick Facts at a Glance

Recall Date
September 12, 2025
Hazard Level
HIGH
Brand
Private Label Skin Care
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
2 states
At-Risk Groups
GENERAL

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 mel rx Skin, NO DRAMA Benzoyl Peroxide 10% Acne Treatment, 7 oz (201 g). It includes Lot numbers 58170A and 58172A, with an expiration date of September 2025.

The Hazard

The recall stems from chemical contamination due to elevated benzene levels found in the product. Benzene is a known carcinogen, raising concerns about long-term health effects.

Reported Incidents

There have been no reported injuries or incidents associated with this recall. It is classified as a Class II recall, suggesting a potential risk of temporary or medically reversible adverse health consequences.

What to Do

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's recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0666-2025.

Key Facts

  • Recalled product: mel rx Skin, NO DRAMA Benzoyl Peroxide 10% Acne Treatment
  • Recall date: September 12, 2025
  • Distribution: California and Georgia
  • Lot numbers: 58170A, 58172A
  • Expiration date: September 2025

Safety Assessment

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

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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