Home NDC 79903-443-08 Regular Strength Stomach Relief
Product NDC 79903-443
Requested package NDC 79903-443-08
11-digit product format 799030443
Labeler code 79903
Product ID 79903-443_57420071-c511-ec7f-e063-6294a90a18e8
Type HUMAN OTC DRUG
Nonproprietary name Bismuth Subsalicylate
Dosage form SUSPENSION
Route ORAL
Labeler Walmart Inc.
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-20
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 Regular Strength 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.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79903-443-08 79903044308 237 mL in 1 BOTTLE (79903-443-08) 237 ml 2026-09-28 No No Current