Systemic Drainage

Product NDC
43742-0647
11-digit product format
437420647
Labeler code
43742
Product ID
43742-0647_2dcc1253-b75f-4e68-93f7-0ff59fe8a6f4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Alfalfa, Avena Sativa, Citrus Limonum, Glycyrrhiza Glabra, Uva-Ursi, Taraxacum Officinale, Galium Aparine, Schisandra Chinensis, Solid Ago Virgaurea, Tabacum, Tylophora Asthmatica, Berberis Vulgaris, Chelidonium Majus, Hepar Suis, Intestine (Suis), Kidney (Suis), Lung (Suis), Lymph Node (Suis), Magnesium Gluconate, Nux Vomica, Potassium Gluconate, Zincum Gluconicum, Sarcolacticum Acidum, Lacticum Acidum
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-11-03
Marketing end
2023-02-22
Substance
ALFALFA; AVENA SATIVA FLOWERING TOP; LEMON JUICE; GLYCYRRHIZA GLABRA; ARCTOSTAPHYLOS UVA-URSI LEAF; TARAXACUM OFFICINALE; GALIUM APARINE; SCHISANDRA CHINENSIS FRUIT; SOLIDAGO VIRGAUREA FLOWERING TOP; TOBACCO LEAF; TYLOPHORA INDICA LEAF; BERBERIS VULGARIS ROOT BARK; CHELIDONIUM MAJUS; PORK LIVER; PORK INTESTINE; PORK KIDNEY; SUS SCROFA LUNG; SUS SCROFA LYMPH; MAGNESIUM GLUCONATE; STRYCHNOS NUX-VOMICA SEED; POTASSIUM GLUCONATE; ZINC GLUCONATE; LACTIC ACID, L-; LACTIC ACID, DL-
Active strength
1 [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; [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS],Seed Storage Proteins [CS],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-0647-14374206470160 mL in 1 BOTTLE, DROPPER (43742-0647-1) 60 ml2015-11-032023-02-22NoNoCurrent