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Private Label Skin Care Inc. Benzoyl Peroxide 10% Acne Treatment Recalled for Benzene Contamination

A benzoyl peroxide acne treatment sold under mel rx Skin by Private Label Skin Care Inc. is recalled for benzene contamination. The recall covers Lot #58170A and 58172A with expiration date 09/2025 and distribution limited to California and Georgia. 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
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
Topical Acne Treatment
Model numbers
Lot # 58170A, Lot # 58172A
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 acne treatment marketed under the mel rx Skin brand. It is a topical pharmaceutical-style product used for acne treatment.

Why This Is Dangerous

Elevated benzene levels present a chemical contamination risk. Benzene exposure can pose health hazards with potential long-term effects.

Industry Context

This recall is not part of a broader industry pattern reported in the data.

Real-World Impact

Immediate stopping of use is required. Consumers may need to seek refunds or replacements. No injuries reported yet, but exposure risk warrants caution.

Practical Guidance

How to identify if yours is affected

  1. Check lot numbers 58170A or 58172A
  2. Check expiration date 09/2025
  3. Verify product label Mel rx Skin NO DRAMA Benzoyl Peroxide 10%

Where to find product info

Label and packaging usually include lot number and expiration date; inspect primary packaging and batch codes.

What timeline to expect

Refund or replacement processing timelines are determined by the company; expect several weeks after eligibility confirmation.

If the manufacturer is unresponsive

  • File a complaint with FDA if regulatory action is needed
  • Seek consumer protection guidance if the company does not respond

How to prevent similar issues

  • Check for benzene-related recalls in cosmetics and OTC products
  • Purchase from reputable retailers with recall outreach practices
  • Register products with brand for recall notifications

Documentation advice

Keep the product, packaging, purchase receipt, and all recall communications. Save photos of labels and batch codes.

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Product Details

Product: mel rx Skin, NO DRAMA Benzoyl Peroxide 10% Acne Treatment. Brand: mel rx Skin. Manufacturer: Private Label Skin Care Inc. Quantity: Not specified. Lot numbers: 58170A, 58172A. Expiration: 09/2025. Distribution: California and Georgia.

Reported Incidents

No injuries or incidents have been reported. The recall is based on benzene findings and regulatory actions.

Key Facts

  • High hazard level due to chemical contamination (benzene).
  • Lot numbers 58170A and 58172A; Exp 09/2025.
  • California and Georgia distribution only.
  • Active recall date: 2025-09-12; Report date: 2025-10-01.

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
POISONINGBURN

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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