Church & Dwight Co., Inc. recalled 21,912 bottles of ZICAM Medicated Fruit Drops on October 1, 2025. The recall stems from a labeling mix-up that failed to disclose elderberry as an ingredient. Consumers should stop using the product immediately.
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Consumers and healthcare providers should stop using this product immediately. Contact Church & Dwight Co., Inc. or your healthcare provider for guidance. Notification method: Letter
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The recall involves ZICAM Medicated Fruit Drops in elderberry flavor, distributed by Church & Dwight Co., Inc. The product was sold in 25-drop bottles with lot number BE51396303 and an expiration date of May 2027.
The labeling issue misrepresents the product's ingredients. Consumers may unknowingly ingest elderberry, which could pose risks for those allergic to it.
There have been no reported injuries or incidents related to this recall. The classification is considered Class II.
Stop using the product immediately. Contact Church & Dwight Co., Inc. for further guidance on the recall.
For more information, call Church & Dwight Co., Inc. or visit their website. Additional details are available on the FDA enforcement page.
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