Home NDC 0220-2127 Filix mas
Product NDC 0220-2127
11-digit product format 002202127
Labeler code 0220
Product ID 0220-2127_1ba85da8-ca87-1104-e063-6294a90a082f
Type HUMAN OTC DRUG
Nonproprietary name DRYOPTERIS FILIX-MAS ROOT
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance DRYOPTERIS FILIX-MAS ROOT
Active strength 30 [hp_C]/30[hp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Filix mas
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DRYOPTERIS FILIX-MAS ROOT 30 [hp_C]/30[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C0ZK0RRF5X 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 0220-2127-41 Filix mas 30 [hp_C] in 1 TUBE PELLET 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-2127 FILIX MAS (DRYOPTERIS FILIX-MAS ROOT) PELLET [BOIRON] 4 Current NDC, Legacy NDC, 1 package rows 20240625_7a40cfae-e34a-306f-e053-2991aa0ab1e1.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 0220-2127-41 00220212741 30 [hp_C] in 1 TUBE (0220-2127-41) 1983-03-03 0000-00-00 No No Current