Homeoplex F (Supplement Clinic, LLC.)


Welcome to the PulseAid listing for the Homeoplex F drug offered from Supplement Clinic, LLC.. 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: Supplement Clinic, LLC.
NON-PROPRIETARY NAME: Echinacea (Angustifolia), Phytolacca Decandra, Lymph Node (Suis), Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum, Kali Muriaticum, Lachesis Mutus, Silicea
SUBSTANCE NAME: ECHINACEA ANGUSTIFOLIA; PHYTOLACCA AMERICANA ROOT; SUS SCROFA LYMPH; CONIUM MACULATUM FLOWERING TOP; FERROUS IODIDE; CALCIUM SULFIDE; POTASSIUM CHLORIDE; LACHESIS MUTA VENOM; SILICON DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2017-11-01
END MARKETING DATE: 0000-00-00


Homeoplex F HUMAN OTC DRUG Details:

Item DescriptionHomeoplex F from Supplement Clinic, LLC.
LABELER NAME: Supplement Clinic, LLC.
DEA SCHEDULE:
ACTIVE STRENGTH: 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)
START MARKETING DATE: 2017-11-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 71781-0004_51931414-344f-4ad1-856f-72ba06f03102
PRODUCT NDC: 71781-0004
APPLICATION NUMBER:

Other ECHINACEA ANGUSTIFOLIA; PHYTOLACCA AMERICANA ROOT; SUS SCROFA LYMPH; CONIUM MACULATUM FLOWERING TOP; FERROUS IODIDE; CALCIUM SULFIDE; POTASSIUM CHLORIDE; LACHESIS MUTA VENOM; SILICON DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Energique, Inc.Lymphapar
Supplement Clinic, LLC.Homeoplex F