Home NDC 0220-3821-41 ORNITHOGALUM UMBELLATUM
Product NDC 0220-3821
Requested package NDC 0220-3821-41
11-digit product format 002203821
Labeler code 0220
Product ID 0220-3821_3a9d84ea-4e24-5f68-e063-6394a90a2abe
Type HUMAN OTC DRUG
Nonproprietary name ORNITHOGALUM UMBELLATUM WHOLE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance ORNITHOGALUM UMBELLATUM WHOLE
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ORNITHOGALUM UMBELLATUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ORNITHOGALUM UMBELLATUM WHOLE 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 9NS3M2Y78S Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-3821-41 ORNITHOGALUM UMBELLATUM 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 0220-3821-41 00220382141 200 [kp_C] in 1 TUBE (0220-3821-41) 2025-01-01 No No Current