dg health stomach relief

Product NDC
55910-800
11-digit product format
559100800
Labeler code
55910
Product ID
55910-800_2f1c5947-4e1a-48cf-8b54-8c3556ec678c
Type
HUMAN OTC DRUG
Nonproprietary name
Bismuth subsalicylate
Dosage form
SUSPENSION
Route
ORAL
Labeler
Dolgencorp Inc
Application
part335
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-09-09
Marketing end
0000-00-00
Substance
BISMUTH SUBSALICYLATE
Active strength
1050 mg/30mL
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 productproduct55910-800DDiscontinued by firm2026-10-05
excluded packagepackage55910-80055910-800-34DDiscontinued 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 · 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 packagepackage55910-800-34d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage55910-800-34f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage55910-800-342ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage55910-800-34a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage55910-800-34cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage55910-800-34cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage55910-800-34302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage55910-800-34ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage55910-800-340efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage55910-800-34ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage55910-800-34367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage55910-800-34557ba5c1ecfa…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
BISMUTH SUBSALICYLATEACTIVE INGREDIENT62TEY51RR1DG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
BISMUTH CATIONACTIVE MOIETYZS9CD1I8YEDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
D&C RED NO. 22INACTIVE INGREDIENT1678RKX8RTDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
D&C RED NO. 28INACTIVE INGREDIENT767IP0Y5NHDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
MAGNESIUM ALUMINUM SILICATEINACTIVE INGREDIENT6M3P64V0NCDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
METHYL SALICYLATEINACTIVE INGREDIENTLAV5U5022YDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
SALICYLIC ACIDINACTIVE INGREDIENTO414PZ4LPZDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
SODIUM SALICYLATEINACTIVE INGREDIENTWIQ1H85SYPDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
SORBIC ACIDINACTIVE INGREDIENTX045WJ989BDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
WATERINACTIVE INGREDIENT059QF0KO0RDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2
XANTHAN GUMINACTIVE INGREDIENTTTV12P4NEEDG HEALTH STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [DOLGENCORP INC]2