Johnson & Johnson recalls Neutrogena Ultra Sheer body mist sunscreen with SPF 100+ due to cGMP deviations. Consumers should check product details and contact the company for instructions.
cGMP Deviations
Johnson & Johnson is recalling Neutrogena Ultra Sheer body mist sunscreen with SPF 100+ because of manufacturing quality control issues. This recall does not involve immediate safety risks but requires consumers to stop using the product and contact the company for further instructions.
The sunscreen was manufactured with deviations in current good manufacturing practices (cGMP). This means the product may not meet quality standards, but it does not pose an immediate risk of injury or illness.
Anyone who owns or uses the Neutrogena Ultra Sheer body mist sunscreen with SPF 100+ is affected. People who apply sunscreen daily are most at risk due to the product's high SPF.
Check for the product name 'Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 100+' on the can. The product includes ingredients like Avobenzone (3%), Homosalate (15%), and Octisalate (5%).
Look for the product name and ingredients listed on the can to confirm if it matches the recalled items.
Reach out to Johnson & Johnson Consumer, Inc. for specific instructions on what to do with the product.
The recall is due to manufacturing quality control issues, not an immediate safety risk. The product is safe to use but should be stopped and returned as per the company's instructions.
Check the can for the product name 'Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 100+' and the ingredients listed.
Contact Johnson & Johnson Consumer, Inc. for specific instructions on how to handle the product.
We’ve drafted a message you can send Neutrogena to request your refund or repair — edit it as you like.
Subject: Recall D-0839-2021 — Neutrogena Neutrogena Hello, I own a Neutrogena that is covered by recall D-0839-2021 from Neutrogena. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
