Home NDC 0220-1852 Echinacea angustifolia
Product NDC 0220-1852
11-digit product format 002201852
Labeler code 0220
Product ID 0220-1852_0a0ca58e-c4fe-ab5b-e063-6394a90ab630
Type HUMAN OTC DRUG
Nonproprietary name ECHINACEA ANGUSTIFOLIA
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance ECHINACEA ANGUSTIFOLIA
Active strength 4 [hp_X]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Echinacea angustifolia
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA ANGUSTIFOLIA 4 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination VB06AV5US8 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 0220-1852-41 Echinacea angustifolia 80 in 1 TUBE PELLET 80 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-1852 ECHINACEA ANGUSTIFOLIA PELLET [BOIRON] 4 Current NDC, Legacy NDC, 1 package rows 20231114_34c51f10-2a55-11e7-82ca-424c58303031.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 Units Marketing start Marketing end Sample Exclude flag Status 0220-1852-41 00220185241 80 PELLET in 1 TUBE (0220-1852-41) 80 pellet 1983-03-03 0000-00-00 No No Current