ZICAM" MEDICATED FRUIT DROPS ELDERBERRY FLAVOR — Class II drug recall D-0095-2026
Ongoing recall by Church & Dwight Co., Inc., reported 2025-10-29, distributed nationwide. Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inc
| Recall number | D-0095-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Church & Dwight Co., Inc., Ewing, NJ, United States |
| Recall initiated | 2025-10-01 |
| Classified | 2025-10-22 |
| Reported by FDA | 2025-10-29 |
| Distributed | Nationwide (US) |
| Quantity | 21,912 bottles |
| Reason classes | labeling |
| NDC | 10237-0469, 10237-0469-22, 10237-0469-25 |
| Lot numbers | 2027/05, BE51396303 |
Product
ZICAM" MEDICATED FRUIT DROPS ELDERBERRY FLAVOR, 25-drops per bottle, Distributed by: Church & Dwight Co., Inc. Ewing, NJ 08628, NDC 10237-469-25
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0095-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.