Home NDC 0220-2582 Hypericum perforatum
Product NDC 0220-2582
11-digit product format 002202582
Labeler code 0220
Product ID 0220-2582_476ac68b-041a-1698-e063-6294a90a7fdf
Type HUMAN OTC DRUG
Nonproprietary name HYPERICUM PERFORATUM
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance HYPERICUM PERFORATUM
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Hypericum perforatum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYPERICUM PERFORATUM 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 XK4IUX8MNB 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 0220-2582-41 Hypericum perforatum 200 [kp_C] in 1 TUBE PELLET 200 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-2582 HYPERICUM PERFORATUM (HYPERICUM PERFORATUM ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230121_85cab607-c6b6-c28e-e053-2a91aa0adf57.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 0220-2582-41 00220258241 200 [kp_C] in 1 TUBE (0220-2582-41) 1983-03-03 0000-00-00 No No Current