Why it was recalled
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Product description
ZICAM" MEDICATED FRUIT DROPS ELDERBERRY FLAVOR, 25-drops per bottle, Distributed by: Church & Dwight Co., Inc. Ewing, NJ 08628, NDC 10237-469-25
Lot numbers, UPCs & expiration codes
Lot#: BE51396303, Exp. Date 2027/05
Where it was sold
Product was distributed nationwide within the United States
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0095-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Oct 1, 2025
- FDA report date
- Oct 29, 2025
- Quantity
- 21,912 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Church & Dwight Co., Inc.
Original FDA data
Every field from FDA enforcement report D-0095-2026, exactly as published.
Show all FDA fields
- City
- Ewing
- State
- NJ
- Status
- Ongoing
- Country
- United States
- Event ID
- 97729
- Address
- 500 Charles Ewing Blvd
- Code information
- Lot#: BE51396303, Exp. Date 2027/05
- Postal code
- 08628-3448
- Report date
- Oct 29, 2025
- Product type
- Drugs
- Recall number
- D-0095-2026
- Classification
- Class II
- Recalling firm
- Church & Dwight Co., Inc.
- Product quantity
- 21,912 bottles
- Reason for recall
- Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- ZICAM" MEDICATED FRUIT DROPS ELDERBERRY FLAVOR, 25-drops per bottle, Distributed by: Church & Dwight Co., Inc. Ewing, NJ 08628, NDC 10237-469-25
- Distribution pattern
- Product was distributed nationwide within the United States
- Recall initiation date
- Oct 1, 2025
- Initial firm notification
- Letter
- Center classification date
- Oct 22, 2025