Scrophularitone (Energique, Inc.)


Welcome to the PulseAid listing for the Scrophularitone drug offered from Energique, Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Energique, Inc.
NON-PROPRIETARY NAME: Baptisia Tinctoria, Echinacea (Angustifolia), Trifolium Pratense, Phytolacca Decandra, Arsenicum Iodatum, Baryta Carbonica, Bromium, Calcarea Carbonica, Kali Muriaticum, Lachesis Mutus, Mercurius Solu
SUBSTANCE NAME: BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA; TRIFOLIUM PRATENSE FLOWER; PHYTOLACCA AMERICANA ROOT; ARSENIC TRIIODIDE; BARIUM CARBONATE; BROMINE; POTASSIUM CHLORIDE; LACHESIS MUTA VENOM; MERCURIUS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2016-03-30
END MARKETING DATE: 0000-00-00


Scrophularitone HUMAN OTC DRUG Details:

Item DescriptionScrophularitone from Energique, Inc.
LABELER NAME: Energique, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 3; 3; 6; 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)
START MARKETING DATE: 2016-03-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 44911-0335_e025c51b-356c-483a-8460-3c98a0adcfe7
PRODUCT NDC: 44911-0335
APPLICATION NUMBER:

Other BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA; TRIFOLIUM PRATENSE FLOWER; PHYTOLACCA AMERICANA ROOT; ARSENIC TRIIODIDE; BARIUM CARBONATE; BROMINE; POTASSIUM CHLORIDE; LACHESIS MUTA VENOM; MERCURIUS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Energique, Inc.Scrophularitone