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Unrated Drug recall · FDA · Published February 23, 2018

Coppertone Kids Sunscreen Spray Recalled for Label Mix-Up

Bayer recalls 528 units of Coppertone Kids Sunscreen Spray (8.3 oz) due to a labeling mix-up. Sold in Arkansas with lots 7N04CS and 7N05CS.

🇺🇸 FDA recall #D-0590-2018DrugCoppertone ›
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Recalling firmBayer HealthCare Pharmaceuticals, Inc.100 Bayer Blvd · Whippany, NJ 07981-1544
✎ GovInfoNow plain-language explainer

What happened, in plain English

Bayer HealthCare Pharmaceuticals is recalling a small batch of Coppertone Kids Sunscreen Spray because the label may not match the product inside. The recall affects only 528 units distributed in Arkansas. The specific nature of the labeling error is described simply as a 'Label mix-up' without further detail on the consequences. Read more at govinfonow.com/recall/40801-coppertone-kids-sunscreen-spray-recalled-for-label-mix-up.

Source Summary by GovInfoNow · govinfonow.com/recall/40801-coppertone-kids-sunscreen-spray-recalled-for-label-mix-up · Updated October 11, 2026 · FDA enforcement record: FDA #D-0590-2018

Cite this page

“Coppertone Kids Sunscreen Spray Recalled for Label Mix-Up.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/40801-coppertone-kids-sunscreen-spray-recalled-for-label-mix-up. Based on FDA recall #D-0590-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0590-2018%22&limit=1).

Why it’s dangerous

The hazard is identified as a labeling mix-up, meaning the information on the bottle may be incorrect or mismatched with the contents. It is unclear from the record whether this results in the wrong ingredients being applied or simply incorrect usage instructions.

Who’s affected

Parents or guardians in Arkansas who purchased Coppertone Kids Sunscreen Spray between the manufacture dates and expiration of November 2019. The record does not specify which age group is most at risk, only that it is a 'Kids' product.

How to tell if you have this one

Check for Coppertone Kids Sunscreen Spray (8.3 oz) bottles distributed by Bayer Healthcare LLC in Whippany, NJ. Look for UPC 41100573636 and Lot numbers 7N04CS or 7N05CS with an expiration date of 11/2019.

  • Brand
    Coppertone
  • Product
    Bayer HealthCare Pharmaceuticals, Inc. recalls Coppertone Kids Sunscreen Spray (avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 4%, Oxybenzone 5%)…
  • Category
    Drug

Where it went and when

Where it was distributed

Distributed in Arkansas.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Arkansas only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arkansas.

Recall timeline

FDA terminated this recall 23 months after the firm started it.

1. Firm started the recall: Feb 23, 201812. FDA classified it Class II: Mar 12, 201823. Published in FDA’s Enforcement Report: Mar 14, 201834. FDA terminated the recall: Jan 9, 2020420182020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Questions people ask

Where was this product sold?

The distribution pattern was Arkansas only.

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Where this comes from

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.

  • Official source: FDA Recall #D-0590-2018 (February 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0590-2018 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA