Home NDC 0220-4631 Selenium metallicum
Product NDC 0220-4631
11-digit product format 002204631
Labeler code 0220
Product ID 0220-4631_0a24cdf7-e451-1d70-e063-6394a90a8826
Type HUMAN OTC DRUG
Nonproprietary name SELENIUM
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance SELENIUM
Active strength 12 [hp_C]/12[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 Selenium metallicum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SELENIUM 12 [hp_C]/12[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H6241UJ22B Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 0220-4631-41 Selenium metallicum 12 [hp_C] in 1 TUBE PELLET 12 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-4631 SELENIUM METALLICUM (SELENIUM) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231115_86d0b78c-675e-5ecb-e053-2991aa0a3067.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 0220-4631-41 00220463141 12 [hp_C] in 1 TUBE (0220-4631-41) 1983-03-03 0000-00-00 No No Current