FDA MedWatch - Specific NEUTROGENA and AVEENO Aerosol Sunscreen Products by Johnson & Johnson:

Recall - Due to Presence of Benzene

MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: Specific NEUTROGENA and AVEENO Aerosol Sunscreen Products by Johnson & Johnson: Recall - Due to Presence of Benzene AUDIENCE: Consumer, Health Professional, Pharmacy  ISSUE: Johnson & Johnson Consumer Inc. is recalling all lots of five NEUTROGENA and AVEENO aerosol sunscreen product lines because internal testing identified low levels of benzene in some samples of the products.  The only sunscreen products impacted are aerosol products, specifically: NEUTROGENA Beach Defense aerosol sunscreen NEUTROGENA Cool Dry Sport aerosol sunscreen NEUTROGENA Invisible Daily defense aerosol sunscreen NEUTROGENA Ultra Sheer aerosol sunscreen AVEENO Protect + Refresh aerosol sunscreen For more information about this recall, click on the red button "Read Recall" below. BACKGROUND: Benzene is classified as a human carcinogen, a substance that could potentially cause cancer depending on the level and extent of exposure. RECOMMENDATIONS:  Consumers should stop using these specific products and appropriately discard them. Consumers should contact their physician or healthcare provider if they have any questions, concerns or have experienced any problems related to using these aerosol sunscreen products. It is important that people everywhere continue to take appropriate sun protection measures, including the continued use of alternative sunscreen. Health professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program: Complete and submit the report online. Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on form, or submit by fax to 1-800-FDA-0178.

Manage Subscriptions  |  Unsubscribe All  |  Help

This email was sent to ooseims.archieves@blogger.com using GovDelivery Communications Cloud on behalf of: U.S. Food and Drug Administration ·  10903 New Hampshire Ave · Silver Spring, MD ·  20993-0002 ·  1-888-INFO-FDA