Stomach Relief

Product NDC
63941-736
Requested package NDC
63941-736-08
11-digit product format
639410736
Labeler code
63941
Product ID
63941-736_1397da35-746d-49aa-962d-8b5fab330ba3
Type
HUMAN OTC DRUG
Nonproprietary name
Bismuth subsalicylate
Dosage form
LIQUID
Route
ORAL
Labeler
Best Choice (Valu Merchandisers Company)
Application
part335
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-12-27
Marketing end
0000-00-00
Substance
BISMUTH SUBSALICYLATE
Active strength
525 mg/30mL
Pharmacologic classes
Bismuth [CS], Bismuth [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage63941-73663941-736-08DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63941-736STOMACH RELIEF (BISMUTH SUBSALICYLATE) LIQUID [BEST CHOICE (VALU MERCHANDISERS COMPANY)]5Legacy NDC20240221_960268c6-7483-4e86-8786-dcd9d39560cc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63941-736-0863941073608473 mL in 1 BOTTLE, PLASTIC (63941-736-08) 473 ml2019-12-270000-00-00NoNoCurrent