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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

Zicam Medicated Fruit Drops Elderberry Flavor Recalled for Label Mix-up

Agency Publication Date: October 22, 2025
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Summary

Church & Dwight Co., Inc. is recalling 21,912 bottles of Zicam Medicated Fruit Drops Elderberry Flavor because of a label mix-up. The product contains elderberry, but the label fails to list it as an ingredient, which poses a serious risk to individuals with allergies or sensitivities to elderberry. This recall affects one specific lot of 25-count bottles distributed nationwide in the United States.

Risk

The product contains elderberry as an ingredient, but the packaging label does not disclose it. Consumers with an allergy or severe sensitivity to elderberry run the risk of a serious or life-threatening allergic reaction if they consume this product.

What You Should Do

  1. Check your bottle for Zicam Medicated Fruit Drops Elderberry Flavor (25 drops per bottle) with Lot Number BE51396303 and an Expiration Date of 2027/05.
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact Church & Dwight Co., Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Zicam Medicated Fruit Drops Elderberry Flavor (25-drops)
Variants: Elderberry Flavor
Lot Numbers:
BE51396303 (Exp 2027/05)
NDC:
10237-469-25

Recall #: D-0095-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97729
Status: Active
Manufacturer: Church & Dwight Co., Inc.
Manufactured In: United States
Units Affected: 21,912 bottles
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.