GILTUSS TOTAL RELEASE

Product NDC
58552-317
Requested package NDC
58552-317-02
11-digit product format
585520317
Labeler code
58552
Product ID
58552-317_c9d5b39b-b35a-3d82-e053-2995a90adb5f
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Gil Pharmaceutical Corp
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2009-10-19
Marketing end
0000-00-00
Substance
PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
Active strength
10 mg/1; mg/1; mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage58552-31758552-317-02DDiscontinued by firm2026-10-05

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 · 15 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31IInactivated by FDA302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20IInactivated by FDAed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10IInactivated by FDA0efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08IInactivated by FDAad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03IInactivated by FDA367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09IInactivated by FDA557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28IInactivated by FDA8af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14IInactivated by FDA834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08IInactivated by FDA1332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
58552-317-012025-06-264060-Gil
58552-317-022025-06-264060-Gil
58552-317-012023-01-304060-Gil
58552-317-022023-01-304060-Gil

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58552-317-01EA - Each58552-31758e6945a-13e5-4514-be70-41bc60de9a3b12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DEXTROMETHORPHAN HYDROBROMIDEACTIVE INGREDIENT9D2RTI9KYHGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
GUAIFENESINACTIVE INGREDIENT495W7451VQGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
PHENYLEPHRINE HYDROCHLORIDEACTIVE INGREDIENT04JA59TNSJGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
DEXTROMETHORPHANACTIVE MOIETY7355X3ROTSGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
GUAIFENESINACTIVE MOIETY495W7451VQGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
PHENYLEPHRINEACTIVE MOIETY1WS297W6MVGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATEINACTIVE INGREDIENTO7TSZ97GEPGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48GILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
HYPROMELLOSE 2910 (6 MPA.S)INACTIVE INGREDIENT0WZ8WG20P6GILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
MAGNESIUM SILICATEINACTIVE INGREDIENT9B9691B2N9GILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30GILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2DGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
MINERAL OILINACTIVE INGREDIENTT5L8T28FGPGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
POVIDONE K30INACTIVE INGREDIENTU725QWY32XGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4GILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPGILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2
TRIACETININACTIVE INGREDIENTXHX3C3X673GILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET [GIL PHARMACEUTICAL CORP]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58552-317GILTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET, FILM COATED EXACTUSS TOTAL RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR, AND PHENYLEPHRINE HCL) TABLET, FILM COATED [GIL PHARMACEUTICAL CORP]5Legacy NDC20210819_a854de22-2f90-48c9-8cde-98446f7958b9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58552-317-025855203170212 BLISTER PACK in 1 CARTON (58552-317-02) > 2 TABLET, FILM COATED in 1 BLISTER PACK12 blister pack2011-07-150000-00-00YesNoCurrent