Johnson & Johnson Consumer recalls Neutrogena Ultra Sheer body mist sunscreen with SPF 45 due to cGMP deviations. Affected products include specific UPCs and sizes. Consumers should check their product details and contact the company for instructions.
cGMP Deviations
Johnson & Johnson Consumer is recalling Neutrogena Ultra Sheer body mist sunscreen with SPF 45 because of cGMP deviations. This means the product may not meet quality standards, but the recall does not specify a risk of injury or harm to users.
The recall is due to cGMP deviations, which are quality control issues in manufacturing. These deviations could mean the sunscreen does not meet the required standards, but the record does not specify how this affects safety or health.
Anyone who owns the Neutrogena Ultra Sheer body mist sunscreen with SPF 45. People who use sunscreen regularly are most at risk if they have the recalled product.
Check for the product name 'Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 45' with specific ingredients and UPC numbers: 0 86800 10039 3 (5 oz) or 0 86800 11134 4 (8 oz).
Look for the product name, ingredients, and UPC numbers listed in the recall notice to confirm if your sunscreen is affected.
The recall states there are cGMP deviations, but the official notice does not specify if the product poses a risk to health or safety.
The recall does not provide a remedy, so you should check the product details and contact Johnson & Johnson Consumer for further instructions.
Check for the product name 'Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 45' with specific UPC numbers: 0 86800 10039 3 (5 oz) or 0 86800 11134 4 (8 oz).
We’ve drafted a message you can send Neutrogena to request your refund or repair — edit it as you like.
Subject: Recall D-0837-2021 — Neutrogena Neutrogena Hello, I own a Neutrogena that is covered by recall D-0837-2021 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.
