NeoCitran Extra Strength — Class II drug recall D-757-2014
Terminated recall by Novartis Consumer Health, reported 2014-01-29, distributed nationwide. Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
| Recall number | D-757-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Novartis Consumer Health, Lincoln, NE, United States |
| Recall initiated | 2013-06-18 |
| Classified | 2014-01-17 |
| Reported by FDA | 2014-01-29 |
| Terminated | 2014-11-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, KR, MX, PA, RU |
| UPC / GTIN / UDI-DI | 00058478100630, 00058478473635 |
| Expiration dates | 2013-07-31, 2013-08-31, 2013-09-30, 2013-12-31, 2014-02-28, 2014-03-31, 2014-05-31, 2014-07-31, 2014-09-30 |
Product
NeoCitran Extra Strength (acetaminophen 650 mg, pseudoephedrine hydrochloride 60 mg, dextromethorphan hydrobromide 20mg, chlorpheniramine maleate 4 mg, ascorbic acid 5 mg) powder packets, Soothing Lemon flavor, 10-single dose pouches per carton, Novartis Consumer Health Canada Inc., Mississauga, ON, labeled as a) NeoCitran Extra Strength Nighttime Total 7 Symptom Relief (UPC 0 58478 10063 0) and b) NeoCitran Extra Strength Cough, Cold & Flu (UPC 0 58478 47363 5).
Reason for recall
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
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-757-2014. 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.