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
ARCTIUM LAPPA ROOT; ARSENIC TRIIODIDE; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; CLEMATIS RECTA FLOWERING TOP; DAPHNE MEZEREUM BARK; ECHINACEA ANGUSTIFOLIA WHOLE; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; GLYCYRRHIZA GLABRA; GOLDENSEAL; GRAPHITE; KEROSENE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SEPIA OFFICINALIS JUICE; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK
Active strength
3; 12; 3; 3; 12; 12; 3; 3; 3; 3; 5; 12; 12; 12; 4; 12; 12; 12; 3; 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_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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
597E9BI3Z3ARCTIUM LAPPA ROOTARCTIUM LAPPA ROOT
3029988O2TARSENIC TRIIODIDE7784-45-4ARSENIC TRIIODIDE
5EF0HWI5WUBAPTISIA TINCTORIA ROOTBAPTISIA TINCTORIA ROOT
1TH8Q20J0UBERBERIS VULGARIS ROOT BARKBERBERIS VULGARIS ROOT BARK
396421SP9FCLEMATIS RECTA FLOWERING TOPCLEMATIS RECTA FLOWERING TOP
X2N6E405GVDAPHNE MEZEREUM BARKDAPHNE MEZEREUM BARK
S2D77IH61RFRANGULA ALNUS BARKFRANGULA ALNUS BARK
4VBP01X99FFRANGULA PURSHIANA BARK8015-89-2FRANGULA PURSHIANA BARK
2788Z9758HGLYCYRRHIZA GLABRA84775-66-6GLYCYRRHIZA GLABRA
ZW3Z11D0JVGOLDENSEALGOLDENSEAL
4QQN74LH4OGRAPHITE7782-42-5GRAPHITE
1C89KKC04EKEROSENE8008-20-6KEROSENE
2E32821G6IOYSTER SHELL CALCIUM CARBONATE, CRUDEOYSTER SHELL CALCIUM CARBONATE, CRUDE
11E6VI8VEGPHYTOLACCA AMERICANA ROOTPHYTOLACCA AMERICANA ROOT
660YQ98I10POTASSIUM CHLORIDE7447-40-7POTASSIUM CHLORIDE
1K573LC5TVPOTASSIUM SULFATE7778-80-5POTASSIUM SULFATE
QDL83WN8C2SEPIA OFFICINALIS JUICESEPIA OFFICINALIS JUICE
4JS0838828TRIFOLIUM PRATENSE FLOWERTRIFOLIUM PRATENSE FLOWER
A4KL1HMZ7TZANTHOXYLUM AMERICANUM BARKZANTHOXYLUM AMERICANUM BARK

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43857-0645-14385706450130 mL in 1 BOTTLE, DROPPER (43857-0645-1) 30 ml2024-12-12NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
DRUG FACTS:BioActive Nutritional, Inc. | Apotheca Company2024-12-12HUMAN OTC DRUG LABEL1