Home NDC 44911-0604 Lymphastat F
Product NDC 44911-0604
11-digit product format 449110604
Labeler code 44911
Product ID 44911-0604_dcf1f69e-2cdb-490c-a769-1c38866801a8
Type HUMAN OTC DRUG
Nonproprietary name Echinacea (Angustifolia), Tabebuia Impetiginosa, Abies Nigra, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (Pratensis), Sepia, Skatolum, Candida Albicans
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-01-04
Marketing end 2027-08-18
Substance ECHINACEA ANGUSTIFOLIA WHOLE; TABEBUIA IMPETIGINOSA BARK; PICEA MARIANA RESIN; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; PULSATILLA PRATENSIS WHOLE; SEPIA OFFICINALIS JUICE; SKATOLE; CANDIDA ALBICANS
Active strength 3; 3; 12; 12; 12; 12; 12; 12; 15; 30 [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], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
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 Lymphastat F Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL PICEA MARIANA RESIN 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL SEPIA OFFICINALIS JUICE 12 [hp_X]/mL SKATOLE 15 [hp_X]/mL CANDIDA ALBICANS 30 [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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0604-1 Lymphastat F 60 mL in 1 BOTTLE, DROPPER LIQUID 60 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0604 LYMPHASTAT F (ECHINACEA (ANGUSTIFOLIA), TABEBUIA IMPETIGINOSA, ABIES NIGRA, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA, SKATOLUM, CANDIDA ALBICANS) LIQUID [ENERGIQUE, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20240307_d41a374c-165c-4408-a8af-bbf6318b10fa.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 Lymphastat F ECHINACEA (ANGUSTIFOLIA), TABEBUIA IMPETIGINOSA, ABIES NIGRA, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA, SKATOLUM, CANDIDA ALBICANS Energique, Inc. d41a374c-165c-4408-a8af-bbf6318b10fa 2024-03-05 Warnings Exact identifier ndc (product): 44911-0604
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0604-1 44911060401 60 mL in 1 BOTTLE, DROPPER (44911-0604-1) 60 ml 2021-01-04 2027-08-18 No No Current