73162-0003 NDC - ENERGY COMPLEX (ECHINACEA (ANGUSTIFOLIA), LAPPA MAJOR, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, ADRENALINUM, ALOE, ARSENICUM ALBUM, BAPTISIA TINCTORIA, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, BRYONIA (ALBA), CHELIDONIUM MAJUS, CROTALUS HORRIDUS, DIGITALIS PURPUREA, FERRUM METALLICUM, GLONOINUM, GLYCYRRHIZA GLABRA, HYDROCOTYLE ASIATICA, IODIUM, IRIS VERSICOLOR, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, RHUS TOX, RUTA GRAVEOLENS, THUJA OCCIDENTALIS, THYROIDINUM (BOVINE))

Drug Information

  • Product NDC: 73162-0003
  • Proprietary Name: Energy Complex
  • Non Proprietary Name: Echinacea (Angustifolia), Lappa Major, Solidago Virgaurea, Taraxacum Officinale, Adrenalinum, Aloe, Arsenicum Album, Baptisia Tinctoria, Berberis Aquifolium, Berberis Vulgaris, Bryonia (Alba), Chelidonium Majus, Crotalus Horridus, Digitalis Purpurea, Ferrum Metallicum, Glonoinum, Glycyrrhiza Glabra, Hydrocotyle Asiatica, Iodium, Iris Versicolor, Lachesis Mutus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Rhus Tox, Ruta Graveolens, Thuja Occidentalis, Thyroidinum (Bovine)
  • Active Ingredient(s): 15 [hp_X]/mL ALOE; 3 [hp_X]/mL ARCTIUM LAPPA ROOT; 15 [hp_X]/mL ARSENIC TRIOXIDE; 15 [hp_X]/mL BAPTISIA TINCTORIA ROOT; 15 [hp_X]/mL BERBERIS VULGARIS ROOT BARK; 15 [hp_X]/mL BRYONIA ALBA ROOT; 15 [hp_X]/mL CENTELLA ASIATICA; 15 [hp_X]/mL CHELIDONIUM MAJUS WHOLE; 15 [hp_X]/mL CROTALUS HORRIDUS HORRIDUS VENOM; 15 [hp_X]/mL DIGITALIS; 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 15 [hp_X]/mL EPINEPHRINE; 15 [hp_X]/mL GLYCYRRHIZA GLABRA; 15 [hp_X]/mL IODINE; 15 [hp_X]/mL IRIS VERSICOLOR ROOT; 15 [hp_X]/mL IRON; 15 [hp_X]/mL LACHESIS MUTA VENOM; 15 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 15 [hp_X]/mL MAHONIA AQUIFOLIUM ROOT BARK; 15 [hp_X]/mL NITROGLYCERIN; 15 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP; 15 [hp_X]/mL SODIUM CHLORIDE; 3 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP; 15 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 3 [hp_X]/mL TARAXACUM OFFICINALE; 15 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG; 15 [hp_X]/mL THYROID, BOVINE; 15 [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]; Allergens [CS]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Nitrate Vasodilator [EPC]; Nitrates [CS]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Vasodilation [PE]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Health Masters LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:2/27/2020

Package Information

No. Package Code Package Description Billing Unit
173162-0003-130 mL in 1 BOTTLE, DROPPER (73162-0003-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73162-0003The 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 NAMEEnergy ComplexThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEchinacea (Angustifolia), Lappa Major, Solidago Virgaurea, Taraxacum Officinale, Adrenalinum, Aloe, Arsenicum Album, Baptisia Tinctoria, Berberis Aquifolium, Berberis Vulgaris, Bryonia (Alba), Chelidonium Majus, Crotalus Horridus, Digitalis Purpurea, Ferrum Metallicum, Glonoinum, Glycyrrhiza Glabra, Hydrocotyle Asiatica, Iodium, Iris Versicolor, Lachesis Mutus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Rhus Tox, Ruta Graveolens, Thuja Occidentalis, Thyroidinum (Bovine)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 DATE2/27/2020This 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 NAMEHealth Masters LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALOE; ARCTIUM LAPPA ROOT; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CENTELLA ASIATICA; CHELIDONIUM MAJUS WHOLE; CROTALUS HORRIDUS HORRIDUS VENOM; DIGITALIS; ECHINACEA ANGUSTIFOLIA WHOLE; EPINEPHRINE; GLYCYRRHIZA GLABRA; IODINE; IRIS VERSICOLOR ROOT; IRON; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MAHONIA AQUIFOLIUM ROOT BARK; NITROGLYCERIN; RUTA GRAVEOLENS FLOWERING TOP; SODIUM CHLORIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; TARAXACUM OFFICINALE; THUJA OCCIDENTALIS LEAFY TWIG; THYROID, BOVINE; 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 STRENGTH15; 3; 15; 15; 15; 15; 15; 15; 15; 15; 3; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 3; 15; 3; 15; 15; 15 
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; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Vasodilation [PE], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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This page was last updated on: 7/25/2025

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