Home NDC 71781-0004-1 Homeoplex F
Product NDC 71781-0004
Requested package NDC 71781-0004-1
11-digit product format 717810004
Labeler code 71781
Product ID 71781-0004_51931414-344f-4ad1-856f-72ba06f03102
Type HUMAN OTC DRUG
Nonproprietary name Echinacea (Angustifolia), Phytolacca Decandra, Lymph Node (Suis), Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum, Kali Muriaticum, Lachesis Mutus, Silicea
Dosage form LIQUID
Route ORAL
Labeler Supplement Clinic, LLC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-11-01
Substance CALCIUM SULFIDE; CONIUM MACULATUM FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; FERROUS IODIDE; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; SILICON DIOXIDE; SUS SCROFA LYMPH
Active strength 12; 12; 3; 12; 12; 3; 12; 12; 6 [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 Increased 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 flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Homeoplex F
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA ANGUSTIFOLIA 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL SUS SCROFA LYMPH 3 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL FERROUS IODIDE 12 [hp_X]/mL CALCIUM SULFIDE 3 [hp_X]/mL POTASSIUM CHLORIDE 12 [hp_X]/mL LACHESIS MUTA VENOM 12 [hp_X]/mL SILICON DIOXIDE 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71781-0004-1 Homeoplex F 60 mL in 1 BOTTLE, DROPPER LIQUID 60 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71781-0004 HOMEOPLEX F (ECHINACEA (ANGUSTIFOLIA), PHYTOLACCA DECANDRA, LYMPH NODE (SUIS), CONIUM MACULATUM, FERRUM IODATUM, HEPAR SULPHURIS CALCAREUM, KALI MURIATICUM, LACHESIS MUTUS, SILICEA) LIQUID [SUPPLEMENT CLINIC, LLC.] 1 Current NDC, Legacy NDC, 1 package rows 20171102_a1872d34-7298-4016-b7b3-830ac1149126.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Homeoplex F ECHINACEA (ANGUSTIFOLIA), PHYTOLACCA DECANDRA, LYMPH NODE (SUIS), CONIUM MACULATUM, FERRUM IODATUM, HEPAR SULPHURIS CALCAREUM, KALI MURIATICUM, LACHESIS MUTUS, SILICEA Supplement Clinic, LLC. a1872d34-7298-4016-b7b3-830ac1149126 2017-11-01 Warnings Exact identifier ndc (package): 71781-0004-1 ndc (product): 71781-0004 ndc11 (package): 71781000401
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71781-0004-1 71781000401 60 mL in 1 BOTTLE, DROPPER (71781-0004-1) 60 ml 2017-11-01 0000-00-00 No No Current