Home NDC 37000-535 Pepto Bismol
Product NDC 37000-535
11-digit product format 370000535
Labeler code 37000
Product ID 37000-535_5d1b51ad-dd9d-d4b1-e063-6394a90a8187
Type HUMAN OTC DRUG
Nonproprietary name Bismuth subsalicylate
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler The Procter & Gamble Manufacturing Company
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-03-01
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 Liquicaps
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBSALICYLATE 262 mg/1
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 37000-535-12 Pepto BismolLiquicaps 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 12 37000-535-12 Pepto BismolLiquicaps 1 in 1 CARTON CAPSULE, LIQUID FILLED 1 12 37000-535-24 Pepto BismolLiquicaps 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 12 37000-535-24 Pepto BismolLiquicaps 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 12 37000-535-48 Pepto BismolLiquicaps 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 12 37000-535-48 Pepto BismolLiquicaps 4 in 1 CARTON CAPSULE, LIQUID FILLED 4 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37000-535 PEPTO BISMOL LIQUICAPS (BISMUTH SUBSALICYLATE) CAPSULE, LIQUID FILLED [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 10 Current NDC, Legacy NDC, 6 package rows 20241011_84ffa6d6-03e1-59e8-e053-2a91aa0afd6e.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 Units Marketing start Marketing end Sample Exclude flag Status 37000-535-12 37000053512 1 BLISTER PACK in 1 CARTON (37000-535-12) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 1 blister pack 2019-03-01 0000-00-00 No No Current 37000-535-24 37000053524 2 BLISTER PACK in 1 CARTON (37000-535-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 2 blister pack 2019-03-01 0000-00-00 No No Current 37000-535-48 37000053548 4 BLISTER PACK in 1 CARTON (37000-535-48) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 4 blister pack 2019-03-01 0000-00-00 No No Current