Home NDC 69842-229-12 Stomach Relief
Product NDC 69842-229
Requested package NDC 69842-229-12
11-digit product format 698420229
Labeler code 69842
Product ID 69842-229_076c8b7c-e4e9-409e-9a90-65c01f4d8047
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form LIQUID
Route ORAL
Labeler CVS Pharmacy
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-31
Substance BISMUTH SUBSALICYLATE
Active strength 525 mg/15mL
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
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 Stomach Relief
Brand name suffix Maximum Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 525 mg/15mL
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 308763 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 69842-229-12 Stomach ReliefMaximum Strength 354 mL in 1 BOTTLE, PLASTIC LIQUID 354 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-229 STOMACH RELIEF MAXIMUM STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [CVS PHARMACY] 7 Current NDC, Legacy NDC, 1 package rows 20240717_9d8f2456-732d-40bf-a10c-98423560c029.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 69842-229-12 69842022912 354 mL in 1 BOTTLE, PLASTIC (69842-229-12) 354 ml 2020-01-31 0000-00-00 No No Current