Church & Dwight recalls ZICAM Elderberry Flavor Drops due to label mix-up not listing elderberry as an ingredient. This affects specific lots and may cause confusion about the product's contents.
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Church & Dwight is recalling ZICAM Medicated Fruit Drops Elderberry Flavor because the label did not correctly list elderberry as an ingredient. This mix-up could lead to confusion about what's actually in the product.
The label failed to indicate that elderberry is an ingredient in the product. This mix-up could cause confusion about what's actually in the bottle, potentially leading to incorrect usage or expectations about the product's effects.
People who bought ZICAM Elderberry Flavor Drops with the specific lot number BE51396303 from the manufacturer are affected. Those using the product for cold or flu symptoms may be at risk of confusion about the ingredients.
Check for the lot number BE51396303 on the bottle. The product is ZICAM Medicated Fruit Drops Elderberry Flavor, 25-drops per bottle, distributed by Church & Dwight Co., Inc. in Ewing, NJ.
Look for the word 'elderberry' on the label to confirm the product's ingredients.
The product is safe to use, but the label mix-up means it may not be clear what ingredients are present. Consult the official recall notice for details.
The recall does not require discarding the product; check the label for elderberry to confirm the ingredients.
Look for the lot number BE51396303 on the bottle. The product is ZICAM Medicated Fruit Drops Elderberry Flavor, 25-drops per bottle, distributed by Church & Dwight Co., Inc. in Ewing, NJ.
We’ve drafted a message you can send Church & Dwight to request your refund or repair — edit it as you like.
Subject: Recall D-0095-2026 — Church & Dwight Church & Dwight Hello, I own a Church & Dwight that is covered by recall D-0095-2026 from Church & Dwight. 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.
