Neutrogena COOLDRY SPORT sunscreen spray with SPF 70 is recalled due to cGMP deviations. This affects all units sold with the specified ingredients and lot numbers. Consumers should contact the manufacturer for details.
cGMP Deviations
Johnson & Johnson Consumer, Inc. has recalled Neutrogena COOLDRY SPORT sunscreen spray SPF 70 due to cGMP deviations. This means the product may not meet quality standards, though no injuries have been reported. The recall covers all units sold with the listed ingredients and lot numbers.
The product was found to have cGMP deviations, which are quality control issues in manufacturing. This could mean the sunscreen does not meet safety and quality standards, though no injuries have been reported. The exact risk level is unclear from the recall notice.
Anyone who owns or uses Neutrogena COOLDRY SPORT sunscreen spray SPF 70. People who have the product with the specified ingredients and lot numbers are most at risk.
Check for the product name 'Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 70' with the listed ingredients. The product is distributed by Johnson & Johnson Consumer, Inc. and has a UPC code 0 86800 10037 9.
Look for the product name, ingredients, and UPC code to confirm if it's recalled.
The recall states there were cGMP deviations, but no injuries have been reported. The product may not meet quality standards, so it's recommended to stop using it until further notice.
Check for the product name 'Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 70' with the listed ingredients and UPC code 0 86800 10037 9.
The recall does not specify a remedy, so contact Johnson & Johnson Consumer, Inc. for further instructions.
We’ve drafted a message you can send Neutrogena to request your refund or repair — edit it as you like.
Subject: Recall D-0835-2021 — Neutrogena Neutrogena Hello, I own a Neutrogena that is covered by recall D-0835-2021 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.
