Home NDC 43857-0645 Epiforce P
Product NDC 43857-0645
11-digit product format 438570645
Labeler code 43857
Product ID 43857-0645_f7bbfab2-45d8-4e99-9d42-685a6d15050f
Type HUMAN OTC DRUG
Nonproprietary name Baptisia Tinctoria, Berberis Vulgaris, Echinacea (Angustifolia), Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Rhamnus Purshiana, Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Hydrastis Canadensis, Arsenicum Iodatum, Calcarea Carbonica, Clematis Erecta, Graphites, Kali Muriaticum, Kali Sulphuricum, Mezereum Petroleum, Sepia
Dosage form LIQUID
Route ORAL
Labeler BioActive Nutritional, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-12-12
Substance BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; ECHINACEA ANGUSTIFOLIA WHOLE; GLYCYRRHIZA GLABRA; ARCTIUM LAPPA ROOT; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK; PHYTOLACCA AMERICANA ROOT; GOLDENSEAL; ARSENIC TRIIODIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CLEMATIS RECTA FLOWERING TOP; GRAPHITE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; DAPHNE MEZEREUM BARK; KEROSENE; SEPIA OFFICINALIS JUICE
Active strength 3; 3; 3; 3; 3; 3; 3; 3; 3; 4; 5; 12; 12; 12; 12; 12; 12; 12; 12; 12 [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_Q]/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], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Plant Proteins [CS], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 Epiforce P
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL GLYCYRRHIZA GLABRA 3 [hp_X]/mL ARCTIUM LAPPA ROOT 3 [hp_X]/mL FRANGULA ALNUS BARK 3 [hp_X]/mL FRANGULA PURSHIANA BARK 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL GOLDENSEAL 5 [hp_Q]/mL ARSENIC TRIIODIDE 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL CLEMATIS RECTA FLOWERING TOP 12 [hp_X]/mL GRAPHITE 12 [hp_X]/mL POTASSIUM CHLORIDE 12 [hp_X]/mL POTASSIUM SULFATE 12 [hp_X]/mL DAPHNE MEZEREUM BARK 12 [hp_X]/mL KEROSENE 12 [hp_X]/mL SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 20 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 43857-0645-1 Epiforce P 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0645 EPIFORCE P (BAPTISIA TINCTORIA, BERBERIS VULGARIS, ECHINACEA (ANGUSTIFOLIA), GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, ARSENICUM IODATUM, CALCAREA CARBONICA, CLEMATIS ERECTA, GRAPHITES, KALI MURIATICUM, KALI SULPHURICUM, MEZEREUM PETROLEUM, SEPIA) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 Current NDC, 1 package rows 20241215_d33282bf-2045-4b92-a377-013fa711c877.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Epiforce P BAPTISIA TINCTORIA, BERBERIS VULGARIS, ECHINACEA (ANGUSTIFOLIA), GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, ARSENICUM IODATUM, CALCAREA CARBONICA, CLEMATIS ERECTA, GRAPHITES, KALI MURIATICUM, KALI SULPHURICUM, MEZEREUM PETROLEUM, SEPIA BioActive Nutritional, Inc. d33282bf-2045-4b92-a377-013fa711c877 2024-12-12 Warnings Exact identifier ndc (product): 43857-0645
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 43857-0645-1 43857064501 30 mL in 1 BOTTLE, DROPPER (43857-0645-1) 30 ml 2024-12-12 No No Current