Home NDC 55505-200 Kaopectate Max Peppermint Flavor Anti Diarrheal
Product NDC 55505-200
11-digit product format 555050200
Labeler code 55505
Product ID 55505-200_28b8a7d7-e01a-4db1-8284-bf48d914eca9
Type HUMAN OTC DRUG
Nonproprietary name bismuth subsalicylate
Dosage form LIQUID
Route ORAL
Labeler Kramer Laboratories
Application M008
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-11-01
Marketing end 2027-01-01
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 Kaopectate Max Peppermint Flavor Anti Diarrheal 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308763 Internal RxNorm lookup 1043048 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 55505-200-36 Kaopectate Max Peppermint Flavor Anti Diarrheal 236 mL in 1 BOTTLE LIQUID 236 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55505-200 KAOPECTATE MAX PEPPERMINT FLAVOR ANTI DIARRHEAL (BISMUTH SUBSALICYLATE) LIQUID [KRAMER LABORATORIES] 4 Current NDC, Legacy NDC, 1 package rows 20241208_e7218045-a593-485b-a5ba-03f3b35cbec4.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 55505-200-36 55505020036 236 mL in 1 BOTTLE (55505-200-36) 236 ml 2020-11-01 2027-01-01 No No Current