NDC 71781-0004

Homeoplex F

Echinacea (angustifolia), Phytolacca Decandra, Lymph Node (suis), Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum, Kali Muriaticum, Lachesis Mutus, Silicea

Homeoplex F is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Supplement Clinic, Llc.. The primary component is Echinacea Angustifolia; Phytolacca Americana Root; Sus Scrofa Lymph; Conium Maculatum Flowering Top; Ferrous Iodide; Calcium Sulfide; Potassium Chloride; Lachesis Muta Venom; Silicon Dioxide.

Product ID71781-0004_51931414-344f-4ad1-856f-72ba06f03102
NDC71781-0004
Product TypeHuman Otc Drug
Proprietary NameHomeoplex F
Generic NameEchinacea (angustifolia), Phytolacca Decandra, Lymph Node (suis), Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum, Kali Muriaticum, Lachesis Mutus, Silicea
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2017-11-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameSupplement Clinic, LLC.
Substance NameECHINACEA ANGUSTIFOLIA; PHYTOLACCA AMERICANA ROOT; SUS SCROFA LYMPH; CONIUM MACULATUM FLOWERING TOP; FERROUS IODIDE; CALCIUM SULFIDE; POTASSIUM CHLORIDE; LACHESIS MUTA VENOM; SILICON DIOXIDE
Active Ingredient Strength3 [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
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71781-0004-1

60 mL in 1 BOTTLE, DROPPER (71781-0004-1)
Marketing Start Date2017-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71781-0004-1 [71781000401]

Homeoplex F LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-01

Drug Details

Active Ingredients

IngredientStrength
ECHINACEA ANGUSTIFOLIA3 [hp_X]/mL

OpenFDA Data

SPL SET ID:a1872d34-7298-4016-b7b3-830ac1149126
Manufacturer
UNII
UPC Code
  • 0745844531135
    • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.