RecallRadar

FDA Drug recall D-754-2014

Theraflu Sugar-Free Nighttime Severe Cold & Cough (acetaminophen 650 mg, diphenhydramine hydrochloride 25 mg, phenylephrine hydrochloride 1…

On 2014-01-29 the FDA classified a Class II recall of Theraflu Sugar-Free Nighttime Severe Cold & Cough (acetaminophen 650 mg, diphenhydramine hydrochloride 25 mg, phenylephrine hydrochloride 1… by Novartis Consumer Health, citing presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-754-2014
ClassificationClass II
Statusterminated
Initiated2013-06-18
Published2014-01-29
Last updated2026-09-13 11:51 UTC
CompanyNovartis Consumer Health
DistributionUS

Product

Theraflu Sugar-Free Nighttime Severe Cold & Cough (acetaminophen 650 mg, diphenhydramine hydrochloride 25 mg, phenylephrine hydrochloride 10 mg) powder packets, Honey Lemon flavor, 6-count packets per carton, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, NDC 0067-6318-06, UPC 3 0043-6318-06 0.

Reason

Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

Identifiers

upc300436318060
code_infoLot #: 10116040, Exp 6/30/2013; 10119871, Exp 7/31/2013; 10122275, Exp 9/30/2013.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-754-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.