Flu Relief Therapy Night Time

Product NDC
55910-154
11-digit product format
559100154
Labeler code
55910
Product ID
55910-154_a4e8dd7d-9be1-473c-b5b1-73284d5fadab
Type
HUMAN OTC DRUG
Nonproprietary name
Theraflu Nighttime
Dosage form
LIQUID
Route
ORAL
Labeler
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2013-07-26
Marketing end
2021-12-30
Substance
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Active strength
325 mg/15mL; mg/15mL; mg/15mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct55910-154DDiscontinued by firm2026-10-12
excluded packagepackage55910-15455910-154-08DDiscontinued by firm2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage55910-154-08d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage55910-154-08f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage55910-154-082ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage55910-154-08a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage55910-154-08cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage55910-154-08cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage55910-154-08302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage55910-154-08ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage55910-154-080efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage55910-154-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage55910-154-08367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage55910-154-08557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AcetaminophenACTIVE INGREDIENT362O9ITL9DFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
DIPHENHYDRAMINE HYDROCHLORIDEACTIVE INGREDIENTTC2D6JAD40FLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
PHENYLEPHRINE HYDROCHLORIDEACTIVE INGREDIENT04JA59TNSJFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
AcetaminophenACTIVE MOIETY362O9ITL9DFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
DIPHENHYDRAMINEACTIVE MOIETY8GTS82S83MFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
PHENYLEPHRINEACTIVE MOIETY1WS297W6MVFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
Acesulfame PotassiumINACTIVE INGREDIENT23OV73Q5G9FLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
AlcoholINACTIVE INGREDIENT3K9958V90MFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
Edetate DisodiumINACTIVE INGREDIENT7FLD91C86KFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOAFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
GlycerinINACTIVE INGREDIENTPDC6A3C0OXFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
MaltitolINACTIVE INGREDIENTD65DG142WKFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3FLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
Sodium BenzoateINACTIVE INGREDIENTOJ245FE5EUFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
Sodium CitrateINACTIVE INGREDIENT1Q73Q2JULRFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RFLU RELIEF THERAPY NIGHT TIME (THERAFLU NIGHTTIME) LIQUID [DOLGENCORP, INC.]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55910-154-0855910015408245 mL in 1 BOTTLE, PLASTIC (55910-154-08) 245 ml2013-07-262021-12-30NoNoCurrent