Home NDC 11673-907 ULTRA STRENGHT PINK BISMUTH
Product NDC 11673-907
11-digit product format 116730907
Labeler code 11673
Product ID 11673-907_42d687a3-14af-be78-e063-6394a90a396b
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form SUSPENSION
Route ORAL
Labeler TARGET CORPORATION
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-10-15
Substance BISMUTH SUBSALICYLATE
Active strength 525 mg/15mL
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 ULTRA STRENGHT PINK BISMUTH
Listing expiration 2026-12-31 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 11673-907-08 ULTRA STRENGHT PINK BISMUTH 236 mL in 1 BOTTLE SUSPENSION 236 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-907 ULTRA STRENGHT PINK BISMUTH (BISMUTH SUBSALICYLATE) SUSPENSION [TARGET CORPORATION] 7 Current NDC, Legacy NDC, 1 package rows 20241109_20063215-f657-487b-9530-6df0181b440a.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 11673-907-08 11673090708 236 mL in 1 BOTTLE (11673-907-08) 236 ml 2019-10-15 0000-00-00 No No Current