TUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION

Product NDC
68998-386
11-digit product format
689980386
Labeler code
68998
Product ID
68998-386_ac9a6897-06d0-444a-b82c-9e00addc487a
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan HBr, Guaifenesin
Dosage form
LIQUID
Route
ORAL
Labeler
Marc Glassman, Inc.
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-08-11
Marketing end
0000-00-00
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
20 mg/10mL; mg/10mL
NDC exclude flag
No
Listing certified through
2020-12-31
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 productproduct68998-386DDiscontinued by firm2026-10-20
excluded packagepackage68998-38668998-386-20DDiscontinued by firm2026-10-20

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 packagepackage68998-386-20d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage68998-386-20f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage68998-386-202ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage68998-386-20a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage68998-386-20cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage68998-386-20cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage68998-386-20302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage68998-386-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage68998-386-200efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage68998-386-20ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage68998-386-20367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage68998-386-20557ba5c1ecfa…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
DEXTROMETHORPHAN HYDROBROMIDEACTIVE INGREDIENT9D2RTI9KYHTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
GUAIFENESINACTIVE INGREDIENT495W7451VQTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
DEXTROMETHORPHANACTIVE MOIETY7355X3ROTSTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
GUAIFENESINACTIVE MOIETY495W7451VQTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS311TUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
CHERRYINACTIVE INGREDIENTBUC5I9595WTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
D&C RED NO. 33INACTIVE INGREDIENT9DBA0SBB0LTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOATUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
HIGH FRUCTOSE CORN SYRUPINACTIVE INGREDIENTXY6UN3QB6STUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
LEVOMENTHOLINACTIVE INGREDIENTBZ1R15MTK7TUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
POVIDONE K30INACTIVE INGREDIENTU725QWY32XTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3TUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
SORBITOLINACTIVE INGREDIENT506T60A25RTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
SUCRALOSEINACTIVE INGREDIENT96K6UQ3ZD4TUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
VANILLAINACTIVE INGREDIENTQ74T35078HTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RTUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1
XANTHAN GUMINACTIVE INGREDIENTTTV12P4NEETUSSIN DM MAX ADULT COUGH PLUS CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [MARC GLASSMAN, INC.]1