Home NDC 0220-5235 VERATRUM VIRIDE
Product NDC 0220-5235
11-digit product format 002205235
Labeler code 0220
Product ID 0220-5235_3b8da0c4-37f2-91ea-e063-6394a90a82a3
Type HUMAN OTC DRUG
Nonproprietary name VERATRUM VIRIDE ROOT
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance VERATRUM VIRIDE 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 VERATRUM VIRIDE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VERATRUM VIRIDE 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 197B3Q7T5Q 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 0220-5235-41 VERATRUM VIRIDE 200 [kp_C] in 1 TUBE PELLET 200 1
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 0220-5235-41 00220523541 200 [kp_C] in 1 TUBE (0220-5235-41) 2025-01-01 No No Current