Home NDC 44911-0739 Hepastat
Product NDC 44911-0739
11-digit product format 449110739
Labeler code 44911
Product ID 44911-0739_5ddeca81-a3fd-4573-ad62-f02e0db5160e
Type HUMAN OTC DRUG
Nonproprietary name Beta Vulgaris, Carduus Marianus, Taraxacum Officinale, Cholesterinum, Cholinum, Fel Tauri, Calcarea Carbonica, Chelidonium Majus, Lycopodium Clavatum, Mercurius Solubilis, Natrum Sulphuricum, Nux Vomica, Phosphorus
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-03-06
Substance BETA VULGARIS WHOLE; BOS TAURUS BILE; CHELIDONIUM MAJUS WHOLE; CHOLESTEROL; CHOLINE HYDROXIDE; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; MILK THISTLE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; TARAXACUM OFFICINALE
Active strength 3; 6; 12; 6; 6; 12; 12; 3; 12; 12; 12; 12; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Hepastat
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BETA VULGARIS WHOLE 3 [hp_X]/mL MILK THISTLE 3 [hp_X]/mL TARAXACUM OFFICINALE 3 [hp_X]/mL CHOLESTEROL 6 [hp_X]/mL CHOLINE HYDROXIDE 6 [hp_X]/mL BOS TAURUS BILE 6 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL CHELIDONIUM MAJUS WHOLE 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL MERCURIUS SOLUBILIS 12 [hp_X]/mL SODIUM SULFATE 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 13 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0739-1 Hepastat 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hepastat BETA VULGARIS, CARDUUS MARIANUS, TARAXACUM OFFICINALE, CHOLESTERINUM, CHOLINUM, FEL TAURI, CALCAREA CARBONICA, CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS Energique, Inc. d9ceea3f-c270-40fa-bf16-d83c683005ac 2026-03-06 Warnings Exact identifier ndc (product): 44911-0739
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 44911-0739-1 44911073901 30 mL in 1 BOTTLE, DROPPER (44911-0739-1) 30 ml 2026-03-06 No No Current