Church & Dwight Co., Inc.: Drug Recall

Recall #D-0095-2026 · 10/01/2025

Class II: Risk

Recall Details

Recall Number
D-0095-2026
Classification
Class II
Product Type
Drug
Recalling Firm
Church & Dwight Co., Inc.
Status
Ongoing
Date Initiated
10/01/2025
Location
Ewing, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated
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.

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

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.