HIGHFDA DRUG

Private Label Skin Care Micronized Benzoyl Peroxide Gel Recall Expands for Benzene Contamination

Private Label Skin Care recalled Micronized BPO Gel Cleanser 10% sold under University Skin Institute in California and Georgia after benzene was detected. The recall is active as of 2025. Consumers should stop using the product 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

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
Micronized Benzoyl Peroxide Gel Cleanser
Model numbers
Lot # 58170A, Lot # 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

This is a benzoyl peroxide gel cleanser marketed for acne treatment. Consumers use it to treat mild to moderate acne on the face or body.

Industry Context

This recall is not described as part of a broader industry pattern in the provided data.

Real-World Impact

Immediate cessation of use is required. No injuries reported yet, but chemical exposure concerns exist for users and healthcare providers.

Practical Guidance

How to identify if yours is affected

  1. Check lot numbers: 58170A and 58172A.
  2. Check expiration date: 09/2025.
  3. Product name: Micronized BPO Gel Cleanser 10% (Benzoyl Peroxide 10%).
  4. Brand: Private Label Skin Care.

Where to find product info

Product packaging and recall notice on FDA enforcement page.

What timeline to expect

Refund or replacement timelines are not specified in the recall notice.

If the manufacturer is unresponsive

  • Contact healthcare providers for guidance.
  • File a consumer complaint with FDA through MedWatch if applicable.

How to prevent similar issues

  • When buying skincare products, verify batch numbers and expiration dates.
  • Purchase from reputable retailers with recall check capabilities.
  • Monitor for any unusual exposure symptoms after use.

Documentation advice

Keep the product, packaging, recall letter, and any medical notes. Save correspondence with the company.

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Product Details

Brand: Private Label Skin Care. Product: Micronized BPO Gel Cleanser 10% (Benzoyl Peroxide 10%). Size: 7 oz (201 g). Lot numbers: 58170A and 58172A. Expiration: 09/2025. Sold at: CA and GA only. Recall date: 2025-09-12. Manufacturer: Private Label Skin Care Inc., or distributed by University Skin Institute, 650 University Ave, Ste 200, Sacramento, CA 95825.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • HIGH hazard level due to chemical contamination with benzene
  • Recall status: ACTIVE as of 2025-10-01
  • Lot numbers: 58170A, 58172A; Exp. 09/2025
  • Distribution limited to CA and GA

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
GENERALPREGNANT
Injury Types
POISONING

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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