Home NDC 0220-3062 Lathyrus sativus
Product NDC 0220-3062
11-digit product format 002203062
Labeler code 0220
Product ID 0220-3062_22ce9866-36bc-c280-e063-6394a90a94ad
Type HUMAN OTC DRUG
Nonproprietary name LATHYRUS SATIVAS SEED
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance LATHYRUS SATIVAS SEED
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 Lathyrus sativus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LATHYRUS SATIVAS SEED 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 8VP54WOT4I 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 0220-3062-41 Lathyrus sativus 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 0220-3062 LATHYRUS SATIVUS (LATHYRUS SATIVAS SEED) PELLET [BOIRON] 2 Current NDC, 1 package rows 20240925_1e698d7d-b34b-eb14-e063-6294a90a2c82.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 0220-3062-41 00220306241 200 [kp_C] in 1 TUBE (0220-3062-41) 2024-01-01 No No Current