Triaminic

Product NDC
0067-8105
11-digit product format
000678105
Labeler code
0067
Product ID
0067-8105_a7817767-c6af-459c-b807-8a7aac951dea
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan HBr, Phenylephrine HCl
Dosage form
SYRUP
Route
ORAL
Labeler
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-10-15
Marketing end
0000-00-00
Substance
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Active strength
5 mg/5mL; mg/5mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 productproduct0067-8105DDiscontinued by firm2026-10-12
excluded packagepackage0067-81050067-8105-04DDiscontinued 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 packagepackage0067-8105-04d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage0067-8105-04f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage0067-8105-042ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage0067-8105-04a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage0067-8105-04cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage0067-8105-04cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage0067-8105-04302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage0067-8105-04ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage0067-8105-040efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage0067-8105-04ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage0067-8105-04367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage0067-8105-04557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0067-8105-04ML - Milliliter0067-81053f888eda-9a80-4fed-a94f-c8c085c844e912013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DEXTROMETHORPHAN HYDROBROMIDEACTIVE INGREDIENT9D2RTI9KYHTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
PHENYLEPHRINE HYDROCHLORIDEACTIVE INGREDIENT04JA59TNSJTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
DEXTROMETHORPHANACTIVE MOIETY7355X3ROTSTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
PHENYLEPHRINEACTIVE MOIETY1WS297W6MVTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
ACESULFAME POTASSIUMINACTIVE INGREDIENT23OV73Q5G9TRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
CHERRYINACTIVE INGREDIENTBUC5I9595WTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86KTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOATRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
MALTITOLINACTIVE INGREDIENTD65DG142WKTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3TRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULRTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RTRIAMINIC DAY TIME COLD AND COUGH (DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) SYRUP [NOVARTIS CONSUMER HEALTH, INC.]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0067-8105-04000678105041 BOTTLE, PLASTIC in 1 CARTON (0067-8105-04) > 118 mL in 1 BOTTLE, PLASTIC2012-10-150000-00-00NoNoCurrent