55714-4814 NDC - EXHAUSTION (ACONITUM NAP., ADRENALINUM, ARALIA QUINQUEFOLIA, ARNICA, ARSENICUM ALB., BAPTISIA, BRYONIA, CANTHARIS, CHELIDONIUM MAJUS, CINCHONA, IODIUM, KALI CARB., KALI IOD., LACHESIS, LYCOPODIUM, LYCOPUS VIRGINICUS, NAT. MUR., NUX VOM., PHOSPHORUS, PULSATILLA, RHUS TOXICODENDRON, SABAL, THYROIDINUM, ECHINACEA, GINGKO, PHYTOLACCA.)

Drug Information

  • Product NDC: 55714-4814
  • Proprietary Name: Exhaustion
  • Non Proprietary Name: Aconitum nap., Adrenalinum, Aralia quinquefolia, Arnica, Arsenicum alb., Baptisia, Bryonia, Cantharis, Chelidonium majus, Cinchona, Iodium, Kali carb., Kali iod., Lachesis, Lycopodium, Lycopus virginicus, Nat. mur., Nux vom., Phosphorus, Pulsatilla, Rhus toxicodendron, Sabal, Thyroidinum, Echinacea, Gingko, Phytolacca.
  • Active Ingredient(s): 20 [hp_X]/mL ACONITUM NAPELLUS; 20 [hp_X]/mL AMERICAN GINSENG; 20 [hp_X]/mL ANEMONE PULSATILLA; 20 [hp_X]/mL ARNICA MONTANA; 20 [hp_X]/mL ARSENIC TRIOXIDE; 20 [hp_X]/mL BAPTISIA TINCTORIA; 20 [hp_X]/mL BRYONIA ALBA ROOT; 20 [hp_X]/mL CHELIDONIUM MAJUS; 20 [hp_X]/mL CINCHONA OFFICINALIS BARK; 11 [hp_X]/mL ECHINACEA, UNSPECIFIED; 20 [hp_X]/mL EPINEPHRINE; 11 [hp_X]/mL GINKGO; 20 [hp_X]/mL IODINE; 20 [hp_X]/mL LACHESIS MUTA VENOM; 20 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 20 [hp_X]/mL LYCOPUS VIRGINICUS; 20 [hp_X]/mL LYTTA VESICATORIA; 20 [hp_X]/mL PHOSPHORUS; 11 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 20 [hp_X]/mL POTASSIUM CARBONATE; 20 [hp_X]/mL POTASSIUM IODIDE; 20 [hp_X]/mL SAW PALMETTO; 20 [hp_X]/mL SODIUM CHLORIDE; 20 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 20 [hp_X]/mL THYROID, UNSPECIFIED; 20 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Catecholamine [EPC]; Catecholamines [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]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Newton Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/2/2019

Package Information

No. Package Code Package Description Billing Unit
155714-4814-130 mL in 1 BOTTLE, GLASS (55714-4814-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55714-4814The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEExhaustionThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAconitum nap., Adrenalinum, Aralia quinquefolia, Arnica, Arsenicum alb., Baptisia, Bryonia, Cantharis, Chelidonium majus, Cinchona, Iodium, Kali carb., Kali iod., Lachesis, Lycopodium, Lycopus virginicus, Nat. mur., Nux vom., Phosphorus, Pulsatilla, Rhus toxicodendron, Sabal, Thyroidinum, Echinacea, Gingko, Phytolacca.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/2/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMENewton Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS; AMERICAN GINSENG; ANEMONE PULSATILLA; ARNICA MONTANA; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS; CINCHONA OFFICINALIS BARK; ECHINACEA, UNSPECIFIED; EPINEPHRINE; GINKGO; IODINE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; LYCOPUS VIRGINICUS; LYTTA VESICATORIA; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE; POTASSIUM IODIDE; SAW PALMETTO; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; THYROID, UNSPECIFIED; TOXICODENDRON PUBESCENS LEAFAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH20; 20; 20; 20; 20; 20; 20; 20; 20; 11; 20; 11; 20; 20; 20; 20; 20; 20; 11; 20; 20; 20; 20; 20; 20; 20 
ACTIVE INGRED UNIT[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; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Catecholamine [EPC], Catecholamines [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], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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This page was last updated on: 12/6/2025

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