Home NDC 0220-4458 Rumex crispus
Product NDC 0220-4458
11-digit product format 002204458
Labeler code 0220
Product ID 0220-4458_f7073903-d494-3ff7-e053-6294a90a6902
Type HUMAN OTC DRUG
Nonproprietary name RUMEX CRISPUS ROOT
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance RUMEX CRISPUS 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 Rumex crispus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RUMEX CRISPUS 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 9N1RM2S62C 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 0220-4458-41 Rumex crispus 200 [kp_C] in 1 TUBE PELLET 200 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-4458 RUMEX CRISPUS (RUMEX CRISPUS ROOT ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230317_86bb1843-8c0b-515d-e053-2991aa0ae6cc.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 0220-4458-41 00220445841 200 [kp_C] in 1 TUBE (0220-4458-41) 1983-03-03 0000-00-00 No No Current