Home NDC 71781-0001 Homeoplex A
Product NDC 71781-0001
11-digit product format 717810001
Labeler code 71781
Product ID 71781-0001_abc6ac3d-e222-4c98-a9cf-1b6dbce52f4a
Type HUMAN OTC DRUG
Nonproprietary name Aralia Quinquefolia, Avena Sativa, Glandula Suprarenalis Suis, Arsenicum Iodatum, Ignatia Amara, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Zincum Metallicum
Dosage form LIQUID
Route ORAL
Labeler Supplement Clinic, LLC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-10-31
Substance AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; SUS SCROFA ADRENAL GLAND; ARSENIC TRIIODIDE; STRYCHNOS IGNATII SEED; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PHOSPHORUS; ZINC
Active strength 3; 3; 6; 12; 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
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Homeoplex A
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMERICAN GINSENG 3 [hp_X]/mL AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL SUS SCROFA ADRENAL GLAND 6 [hp_X]/mL ARSENIC TRIIODIDE 12 [hp_X]/mL STRYCHNOS IGNATII SEED 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL PHOSPHORIC ACID 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL ZINC 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 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 71781-0001-1 Homeoplex A 60 mL in 1 BOTTLE, DROPPER LIQUID 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71781-0001 HOMEOPLEX A (ARALIA QUINQUEFOLIA, AVENA SATIVA, GLANDULA SUPRARENALIS SUIS, ARSENICUM IODATUM, IGNATIA AMARA, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORICUM ACIDUM, PHOSPHORUS, ZINCUM METALLICUM) LIQUID [SUPPLEMENT CLINIC, LLC.] 2 Current NDC, Legacy NDC, 1 package rows 20171101_fee279bf-76b7-4a84-ac8c-cd2489a910fb.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 A ARALIA QUINQUEFOLIA, AVENA SATIVA, GLANDULA SUPRARENALIS SUIS, ARSENICUM IODATUM, IGNATIA AMARA, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORICUM ACIDUM, PHOSPHORUS, ZINCUM METALLICUM Supplement Clinic, LLC. fee279bf-76b7-4a84-ac8c-cd2489a910fb 2017-11-01 Warnings Exact identifier ndc (product): 71781-0001
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71781-0001-1 71781000101 60 mL in 1 BOTTLE, DROPPER (71781-0001-1) 60 ml 2017-10-31 0000-00-00 No No Current