Tinnitus (Newton Laboratories, Inc.)


Welcome to the PulseAid listing for the Tinnitus drug offered from Newton Laboratories, Inc.. This Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Vegetable Proteins [Chemical/Ingredient],Antimalarial [EPC],Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Newton Laboratories, Inc.
NON-PROPRIETARY NAME: Aconitum nap., Baryta carb., Baryta mur., Capsicum, Causticum, Chenopodium anthelminticum, Chininum sulphuricum, Cinchona, Glonoinum, Graphites, Hydrastis, Kali bic., Kali mur., Lycopodium, Phosphorus
SUBSTANCE NAME: ACONITUM NAPELLUS; BARIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; CAPSICUM; CAUSTICUM; DYSPHANIA AMBROSIOIDES; QUININE SULFATE; CINCHONA OFFICINALIS BARK; NITROGLYCERIN; GRAPHITE; GOLDENSEAL; POTASSIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Vegetable Proteins [Chemical/Ingredient],Antimalarial [EPC],Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2011-06-01
END MARKETING DATE: 0000-00-00


Tinnitus HUMAN PRESCRIPTION DRUG Details:

Item DescriptionTinnitus from Newton Laboratories, Inc.
LABELER NAME: Newton Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15([hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g)
START MARKETING DATE: 2011-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 55714-4585_2c8847e3-e129-6b7d-ff3e-832fd636f527
PRODUCT NDC: 55714-4585
APPLICATION NUMBER:

Other ACONITUM NAPELLUS; BARIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; CAPSICUM; CAUSTICUM; DYSPHANIA AMBROSIOIDES; QUININE SULFATE; CINCHONA OFFICINALIS BARK; NITROGLYCERIN; GRAPHITE; GOLDENSEAL; POTASSIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Newton Laboratories, Inc.Tinnitus