NDC 44911-0335

Scrophularitone

Baptisia Tinctoria, Echinacea (angustifolia), Trifolium Pratense, Phytolacca Decandra, Arsenicum Iodatum, Baryta Carbonica, Bromium, Calcarea Carbonica, Kali Muriaticum, Lachesis Mutus, Mercurius Solubilis

Scrophularitone is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Arsenic Triiodide; Baptisia Tinctoria Root; Barium Carbonate; Bromine; Echinacea Angustifolia; Lachesis Muta Venom; Mercurius Solubilis; Phytolacca Americana Root; Potassium Chloride; Trifolium Pratense Flower.

Product ID44911-0335_1148fa93-c689-48b4-93d5-c07ee221468c
NDC44911-0335
Product TypeHuman Otc Drug
Proprietary NameScrophularitone
Generic NameBaptisia Tinctoria, Echinacea (angustifolia), Trifolium Pratense, Phytolacca Decandra, Arsenicum Iodatum, Baryta Carbonica, Bromium, Calcarea Carbonica, Kali Muriaticum, Lachesis Mutus, Mercurius Solubilis
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2016-03-30
Marketing End Date2024-10-24
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameEnergique, Inc.
Substance NameARSENIC TRIIODIDE; BAPTISIA TINCTORIA ROOT; BARIUM CARBONATE; BROMINE; ECHINACEA ANGUSTIFOLIA; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; TRIFOLIUM PRATENSE FLOWER
Active Ingredient Strength12 [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
Pharm ClassesIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC Exclude FlagN

Packaging

NDC 44911-0335-1

30 mL in 1 BOTTLE, DROPPER (44911-0335-1)
Marketing Start Date2016-03-30
Marketing End Date2024-10-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 44911-0335-1 [44911033501]

Scrophularitone LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-03-30

Drug Details

Active Ingredients

IngredientStrength
BAPTISIA TINCTORIA ROOT3 [hp_X]/mL

OpenFDA Data

SPL SET ID:02ffd451-01a9-4512-b770-87e24a9a6853
Manufacturer
UNII

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