PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold — Class III drug recall D-1352-2014
Terminated recall by Prestige Brands Holdings, reported 2014-06-04, distributed nationwide. Presence of Precipitate; small amounts of diphenhydramine precipitated out of solution
| Recall number | D-1352-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Prestige Brands Holdings, Tarrytown, NY, United States |
| Recall initiated | 2014-04-25 |
| Classified | 2014-05-28 |
| Reported by FDA | 2014-06-04 |
| Terminated | 2015-09-15 |
| Distributed | Nationwide (US) |
| Lot numbers | 133196, 144273, 154090, 73242, 73243, 73244, 73824, 74207, 74303, 74460, 78805, 79265, 79266, 79573, 80456, 80457, 83746 |
Product
PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold, (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL OZ (118 mL), Distributed by Medtech Products, Inc., Tarrytown,NY ---- UPC 814832013544
Reason for recall
Presence of Precipitate; small amounts of diphenhydramine precipitated out of solution
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-1352-2014. 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.