Home NDC 0220-0606 Artemisia vulgaris
Product NDC 0220-0606
11-digit product format 002200606
Labeler code 0220
Product ID 0220-0606_253c9d92-7556-4429-e063-6394a90a52f1
Type HUMAN OTC DRUG
Nonproprietary name ARTEMISIA VULGARIS ROOT
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance ARTEMISIA VULGARIS 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 Artemisia vulgaris
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARTEMISIA VULGARIS 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 32MP823R8S 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 0220-0606-41 Artemisia vulgaris 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 0220-0606 ARTEMISIA VULGARIS (ARTEMISIA VULGARIS ROOT) PELLET [BOIRON] 1 Current NDC, 1 package rows 20241027_253c9d92-7555-4429-e063-6394a90a52f1.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 0220-0606-41 00220060641 200 [kp_C] in 1 TUBE (0220-0606-41) 2024-01-01 No No Current