Home NDC 85237-1903-7 Pepto Bismol
Product NDC 85237-1903
Requested package NDC 85237-1903-7
11-digit product format 852371903
Labeler code 85237
Product ID 85237-1903_5611c6cb-5c0c-cf4e-e063-6394a90abff8
Type HUMAN OTC DRUG
Nonproprietary name Bismuth Subsalicylate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Select Consumer Group
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-06-30
Substance BISMUTH SUBSALICYLATE
Active strength 262 mg/1
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 Pepto Bismol
Brand name suffix CHEWABLES
Listing expiration 2027-12-31 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 211151 Internal RxNorm lookup 308761 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 85237-1903-7 85237190307 3 POUCH in 1 CARTON (85237-1903-7) / 2 TABLET, CHEWABLE in 1 POUCH (85237-1903-0) 3 pouch 2025-07-08 No No Current