Home NDC 0220-0609 Arum maculatum
Product NDC 0220-0609
11-digit product format 002200609
Labeler code 0220
Product ID 0220-0609_15ac75cb-ae0f-afb9-e063-6394a90a4679
Type HUMAN OTC DRUG
Nonproprietary name ARUM MACULATUM ROOT
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance ARUM MACULATUM ROOT
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 Arum maculatum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARUM MACULATUM ROOT 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 646O39K8BJ 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 0220-0609-41 Arum maculatum 200 [kp_C] in 1 TUBE PELLET 200 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0609 ARUM MACULATUM (ARUM MACULATUM ROOT) PELLET [BOIRON] 1 Current NDC, 1 package rows 20240410_15ac75cb-ae0e-afb9-e063-6394a90a4679.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 Sample Exclude flag Status 0220-0609-41 00220060941 200 [kp_C] in 1 TUBE (0220-0609-41) 2024-01-01 No No Current