Home NDC 0220-0860 BISMUTHUM SUBNITRICUM
Product NDC 0220-0860
11-digit product format 002200860
Labeler code 0220
Product ID 0220-0860_39e8a434-0720-b2b0-e063-6294a90acd00
Type HUMAN OTC DRUG
Nonproprietary name BISMUTH SUBNITRATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance BISMUTH SUBNITRATE
Active strength 200 [kp_C]/200[kp_C]
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base BISMUTHUM SUBNITRICUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISMUTH SUBNITRATE 200 [kp_C]/200[kp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H19J064BA5 Internal UNII 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 0220-0860-41 BISMUTHUM SUBNITRICUM 200 [kp_C] in 1 TUBE PELLET 200 1
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 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 0220-0860-41 00220086041 200 [kp_C] in 1 TUBE (0220-0860-41) 2025-01-01 No No Current