Home NDC 69618-029 Bismuth Subsalicylate 262 mg
Product NDC 69618-029
11-digit product format 696180029
Labeler code 69618
Product ID 69618-029_2bc8473d-ad00-da1d-e063-6394a90ae0d4
Type HUMAN OTC DRUG
Nonproprietary name Bismuth Subsalicylate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Reliable 1 Laboratories LLC
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-11-01
Substance BISMUTH SUBSALICYLATE
Active strength 262 mg/1
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 Bismuth Subsalicylate 262 mg
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 262 mg/1
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 308761 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69618-029-03 Bismuth Subsalicylate 262 mg 30 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 30 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69618-029 BISMUTH SUBSALICYLATE 262 MG (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [RELIABLE 1 LABORATORIES LLC] 6 Current NDC, Legacy NDC, 1 package rows 20250117_2e40ffd8-1afa-43af-e054-00144ff8d46c.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 4 of 10 · 198 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69618-029-03 69618002903 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (69618-029-03) 2015-11-01 0000-00-00 No No Current