Home NDC 0220-0837 Berberis vulgaris
Product NDC 0220-0837
11-digit product format 002200837
Labeler code 0220
Product ID 0220-0837_f2f3a73d-5be6-36c6-e053-2995a90ac478
Type HUMAN OTC DRUG
Nonproprietary name BERBERIS VULGARIS ROOT BARK
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance BERBERIS VULGARIS ROOT BARK
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 Berberis vulgaris
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BERBERIS VULGARIS ROOT BARK 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 1TH8Q20J0U 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 0220-0837-41 Berberis vulgaris 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 0220-0837 BERBERIS VULGARIS (BERBERIS VULGARIS ROOT BARK ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230124_8500b339-58a2-2152-e053-2991aa0a7815.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 0220-0837-41 00220083741 200 [kp_C] in 1 TUBE (0220-0837-41) 1983-03-03 0000-00-00 No No Current