Home NDC 0220-0942 Bryonia
Product NDC 0220-0942
11-digit product format 002200942
Labeler code 0220
Product ID 0220-0942_476e4934-8215-7942-e063-6294a90a253b
Type HUMAN OTC DRUG
Nonproprietary name BRYONIA ALBA ROOT
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance BRYONIA ALBA ROOT
Active strength 12 [hp_C]/12[hp_C]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Bryonia
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BRYONIA ALBA ROOT 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 T7J046YI2B 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 0220-0942-41 Bryonia 12 [hp_C] in 1 TUBE PELLET 12 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0942 BRYONIA (BRYONIA ALBA ROOT ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231017_8489d328-17e3-317f-e053-2991aa0a87a9.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 0220-0942-41 00220094241 12 [hp_C] in 1 TUBE (0220-0942-41) 1983-03-03 0000-00-00 No No Current