Home NDC 44911-0344 Hypericum
Product NDC 44911-0344
11-digit product format 449110344
Labeler code 44911
Product ID 44911-0344_4fbbade8-ce83-467c-bdc4-1e9181ae8b54
Type HUMAN OTC DRUG
Nonproprietary name Hypericum Perforatum
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-04-12
Substance HYPERICUM PERFORATUM WHOLE
Active strength 200 [hp_C]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Hypericum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYPERICUM PERFORATUM WHOLE 200 [hp_C]/mL
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 44911-0344-1 Hypericum 30 mL in 1 BOTTLE, DROPPER LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0344 HYPERICUM (HYPERICUM PERFORATUM) LIQUID [ENERGIQUE, INC] 5 Current NDC, Legacy NDC, 1 package rows 20240806_2ef4d9c5-0511-4a7b-9431-314c83a4c945.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 Units Marketing start Marketing end Sample Exclude flag Status 44911-0344-1 44911034401 30 mL in 1 BOTTLE, DROPPER (44911-0344-1) 30 ml 2016-04-12 0000-00-00 No No Current