ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly Hills, CA 90210
Summary
The FDA issued a Class II for ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly H by Private Label Skin Care Inc.. Reason: Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoy.
Details
Source
Drug Recall
External ID
D-0663-2025
Action Date
2025-10-01
Status
Ongoing
Category
drug
Product Description
ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly Hills, CA 90210
Lot/Code Info: Lot # 58170A and 58172A, Exp Date: 09/2025
Quantity Affected: 125
Reason for Recall
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Distribution
CA, GA only
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-12
Company
Canoga Park, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 70 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Private Label Skin Care Inc. has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Private Label Skin Care Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Private Label Skin Care Inc. have FDA actions?
Private Label Skin Care Inc. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0663-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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