Home NDC 70000-0045 Stomach Relief Ultra
Product NDC 70000-0045
11-digit product format 700000045
Labeler code 70000
Product ID 70000-0045_336b5b1d-58a5-445c-8e8b-8c7ffdf05852
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form LIQUID
Route ORAL
Labeler CARDINAL HEALTH 110, LLC. DBA LEADER 70000
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-02-25
Marketing end 2026-12-28
Substance BISMUTH SUBSALICYLATE
Active strength 525 mg/15mL
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
NDC exclude flag No
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 Ultra Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 525 mg/15mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0045-1 Stomach Relief Ultra 355 mL in 1 BOTTLE, PLASTIC LIQUID 355 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0045 STOMACH RELIEF ULTRA (BISMUTH SUBSALICYLATE) LIQUID [CARDINAL HEALTH (LEADER) 70000] 4 Current NDC, Legacy NDC, 1 package rows 20240911_5f7a0905-344b-40e1-8b32-171dabb560b3.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 2 of 10 · 198 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 70000-0045-1 70000004501 355 mL in 1 BOTTLE, PLASTIC (70000-0045-1) 355 ml 2020-02-25 2026-12-28 No No Current