← FDA ENFORCEMENT
D-0095-2026Class II

Church & Dwight Co., Inc.

Recalling firm
Church & Dwight Co., Inc.
Product type
Drug
Status
Ongoing
Report date
2025-10-29
Distribution
Product was distributed nationwide within the United States
Firm state
NJ
Product quantity
21,912 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
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

Code / lot info

Lot#: BE51396303, Exp. Date 2027/05

Other recalls SPEQ maps to Documentation & Change Control
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See all Documentation & Change Control recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.