Johnson & Johnson Neutrogena COOLDRY SPORT Sunscreen Spray Recalled
Johnson & Johnson Consumer, Inc. is voluntarily recalling Neutrogena COOLDRY SPORT sunscreen spray (SPF 50) due to cGMP deviations. Approximately 867,816 cans distributed nationwide are affected.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall initiated voluntarily by the firm for cGMP deviations. The source text does not report any illnesses, injuries, or hospitalizations, making this a precautionary recall. Per the rubric, voluntary recalls with no reported harm typically warrant a Moderate (2) rating.
Plain-English summary
Johnson & Johnson Consumer, Inc. is voluntarily recalling Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 50, a 5.0 oz aerosol product containing Avobenzone (3%), Homosalate (10%), Octisalate (5%), and Octocrylene (10%). The recall was initiated on July 14, 2021, and was formally classified by the FDA on September 24, 2021.
The firm initiated this recall due to cGMP (current Good Manufacturing Practices) deviations. All lots within the expiry date are included in this recall.
Approximately 867,816 cans have been distributed nationwide in the United States under UPC 0 86800 10036 2. Consumers should discontinue use and consult the firm or their healthcare provider with questions. The firm notified customers through multiple channels including email, fax, letter, press release, telephone, and direct visits.
The recalled product
- Product
- Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 50, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT 5.0 OZ (141 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 10036 2
- Manufacturer
- Johnson & Johnson Consumer, Inc.
- Category
- Drug — Topical / Sunscreen
- Affected units
- 867,816
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lots within expiry.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 20 recalled by Johnson & Johnson Consumer, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 20 products in this recall →Related recalls
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