HIGH

Church & Dwight Zicam Elderberry Medicated Fruit Drops Recalled for Label Mix-Up (21,912 Bottles, 0

Church & Dwight recalled 21,912 bottles of ZICAM Cold Remedy Medicated Fruit Drops Elderberry from nationwide distribution in the United States. The label did not indicate elderberry as an ingredient though the product contains elderberry. Consumers should stop using the product and contact Church & Dwight for guidance.

Quick Facts at a Glance

Recall Date
October 1, 2025
Hazard Level
HIGH
Brands
Zicam, Church & Dwight
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.

What You Should Do

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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About This Product

Zicam Cold Remedy Medicated Fruit Drops are a flavored lozenge intended to relieve cold symptoms. The elderberry flavor variant is distributed nationwide in the U.S. by Church & Dwight.

Why This Is Dangerous

The problem is a label mix-up. Elderberry is an ingredient in the product, but the label did not disclose this ingredient.

Industry Context

This recall is not indicated as part of a broader industry pattern.

Real-World Impact

Consumers may unknowingly ingest elderberry due to labeling gaps. This could prompt label-related confusion and misinformed use.

Practical Guidance

How to identify if yours is affected

  1. Check the lot number on the bottle BE51396303.
  2. Check the expiration date 2027-05.
  3. Verify the NDC 10237-469-25.
  4. Inspect the label for elderberry listing.

Where to find product info

NDC 10237-469-25; Lot BE51396303; Exp 2027-05; 25 drops per bottle

What timeline to expect

Recall letter will outline next steps for disclosure and disposition of affected product

If the manufacturer is unresponsive

  • Document all contacts with Church & Dwight
  • Consider filing a complaint with consumer protection authorities
  • Consult legal counsel if handling disputes or injuries occur

How to prevent similar issues

  • Always read ingredient listings on OTC products
  • Verify NDC and lot numbers before use
  • Check recall notices on FDA or manufacturer websites
  • Ask healthcare providers about potential ingredient exposures when using medicated products

Documentation advice

Keep the bottle, packaging, all recall letters, and proof of purchase for records

Product Details

Brand: Zicam COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY Product: Medicated fruit drops Size: 25 drops per bottle NDC: 10237-469-25 Lot: BE51396303 Exp: 2027-05 Units recalled: 21,912 bottles Distribution: Nationwide in the United States Distributor: Church & Dwight Co., Inc., Ewing, NJ 08628 Sold at: Unknown Price: Unknown

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 21,912 bottles recalled
  • NDC 10237-469-25
  • Lot BE51396303
  • Exp 2027-05
  • Distributed nationwide in the U.S.
  • Labeling mix-up; elderberry not listed on label

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
BE51396303
Exp 2027-05
UPC Codes
10237-469
10237-469-25
Affected States
ALL
Report Date
October 29, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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