Home NDC 0220-4310 Radium bromatum
Product NDC 0220-4310
11-digit product format 002204310
Labeler code 0220
Product ID 0220-4310_097e16d0-9f84-ba28-e063-6294a90af714
Type HUMAN OTC DRUG
Nonproprietary name RADIUM BROMIDE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance RADIUM BROMIDE
Active strength 15 [hp_C]/15[hp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Radium bromatum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RADIUM BROMIDE 15 [hp_C]/15[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R74O7T8569 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-4310-41 Radium bromatum 15 [hp_C] in 1 TUBE PELLET 15 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-4310 RADIUM BROMATUM (RADIUM BROMIDE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231107_86a9324c-a9a3-3b8d-e053-2a91aa0ae39f.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 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0220-4310-41 00220431041 15 [hp_C] in 1 TUBE (0220-4310-41) 1983-03-03 0000-00-00 No No Current