HIGHFDA DRUG

Private Label Skin Care Benzoyl Peroxide 10% Recall for Benzene Contamination

Private Label Skin Care recalls Artisan of Skin Benzoyl Peroxide 10% cream after benzene detected. The product was distributed in California and Georgia. Consumers should stop use immediately and contact the company for guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
September 12, 2025
Status
ACTIVE
Severity
8/10

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, PREGNANT, PETS

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Private Label Skin Care
Product type
Benzoyl Peroxide Cream
Model numbers
Lot # 58170A, 58172A
Sizes
7 oz (201 g)
Sold at
Unknown
Where affected
CA, GA

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    September 12, 2025

  2. Reported by FDA DRUG

    October 1, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Artisan of Skin Benzoyl Peroxide 10% cream is used for acne treatment. It is sold in small batches by Private Label Skin Care Inc. Typical use involves topical application to affected areas.

Why This Is Dangerous

Benzene contamination poses chemical exposure risk if absorbed through skin or inhaled. Safety guidance emphasizes stopping use.

Industry Context

This recall is not described as part of a broader industry pattern.

Practical Guidance

How to identify if yours is affected

  1. Check bottle for 7 oz size and Lot numbers 58170A or 58172A
  2. Verify expiration date 09/2025
  3. Confirm brand is Artisan of Skin by Private Label Skin Care

Where to find product info

Recall page and FDA enforcement listing; contact Private Label Skin Care Inc. for guidance

What timeline to expect

Remedies and refunds likely arranged through company notification; timelines vary

If the manufacturer is unresponsive

  • Escalate to FDA recall program
  • File a consumer complaint with CPSC if needed
  • Seek legal advice if no remedy offered

How to prevent similar issues

  • Check lot numbers before use
  • Do not purchase from unauthorized sellers
  • Monitor for additional recalls in this product category

Documentation advice

Save recall notification, photos of lot, bottle, and expiration date; retain receipts if available

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Product Details

Product: Artisan of Skin Benzoyl Peroxide 10% Cream. Size: 7 oz (201 g). Brand: Private Label Skin Care. Distribution: California and Georgia. Lot numbers: 58170A and 58172A. Expiration: 09/2025. Recall date: 2025-09-12. Status: ACTIVE.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Lot # 58170A and 58172A
  • Distributed in CA and GA
  • Hazard high: benzene contamination

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETS
Injury Types
POISONINGOTHER

Product Details

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

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