Home NDC 0220-1882-41 EQUISETUM ARVENSE
Product NDC 0220-1882
Requested package NDC 0220-1882-41
11-digit product format 002201882
Labeler code 0220
Product ID 0220-1882_31f66910-b093-aa75-e063-6294a90a1bb0
Type HUMAN OTC DRUG
Nonproprietary name EQUISETUM ARVENSE TOP
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance EQUISETUM ARVENSE TOP
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 EQUISETUM ARVENSE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength EQUISETUM ARVENSE TOP 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 1DP6Y6B65Z 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 0220-1882-41 EQUISETUM ARVENSE 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 0220-1882 EQUISETUM ARVENSE (EQUISETUM ARVENSE TOP) PELLET [BOIRON] 1 Current NDC, 1 package rows 20250406_31f66910-b092-aa75-e063-6294a90a1bb0.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 0220-1882-41 00220188241 200 [kp_C] in 1 TUBE (0220-1882-41) 2024-01-01 No No Current