Home NDC 50804-122 GS Stomach Relief
Product NDC 50804-122
11-digit product format 508040122
Labeler code 50804
Product ID 50804-122_5bf316e3-e707-4464-8757-e2452bacefc9
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate 525 mg
Dosage form LIQUID
Route ORAL
Labeler Good Sense (Geiss, Destin & Dunn, Inc.)
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-10-30
Substance BISMUTH SUBSALICYLATE
Active strength 525 mg/30mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base GS Stomach Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 525 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 62TEY51RR1 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308762 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50804-122-04 GS Stomach Relief 236 mL in 1 BOTTLE LIQUID 236 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50804-122 GS STOMACH RELIEF (BISMUTH SUBSALICYLATE 525 MG) LIQUID [GOOD SENSE (GEISS, DESTIN & DUNN, INC.)] 3 Current NDC, Legacy NDC, 1 package rows 20241222_edd15c7d-f66b-4b1a-8cda-9814a3790483.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 12 · 223 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50804-122-04 50804012204 236 mL in 1 BOTTLE (50804-122-04) 236 ml 2018-10-30 0000-00-00 No No Current