Home NDC 0220-2164 Fucus vesiculosus
Product NDC 0220-2164
11-digit product format 002202164
Labeler code 0220
Product ID 0220-2164_1b19b48b-52ab-7a7b-e063-6294a90abfd5
Type HUMAN OTC DRUG
Nonproprietary name FUCUS VESICULOSUS
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance FUCUS VESICULOSUS
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 Fucus vesiculosus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FUCUS VESICULOSUS 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 535G2ABX9M 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 0220-2164-41 Fucus vesiculosus 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 0220-2164 FUCUS VESICULOSUS PELLET [BOIRON] 2 Current NDC, 1 package rows 20240618_1b18895e-8ed4-675a-e063-6294a90a86a1.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 Sample Exclude flag Status 0220-2164-41 00220216441 200 [kp_C] in 1 TUBE (0220-2164-41) 2024-01-01 No No Current