64578-0172 NDC - LYMPH-TONE III (ADENOSINUM CYCLOPHOSPHORICUM, ARNICA, BOLDO, CALC IOD, CALENDULA, CARTILAGO SUIS, CEANOTHUS, COENZYME A, ECHINACEA, HAMAMELIS, HEPAR SULPH CALC, HYPOTHALAMUS, NADIDUM, NAJA, NAT SULPHURICUM, PHASEOLUS, PHOS, PHYTOLACCA, PINUS SYL, PITUITARUM POSTERIUM, PYROGENIUM, SILICEA, SULPHUR, THUJA OCC, THYROIDINUM, VISCUM)

Drug Information

  • Product NDC: 64578-0172
  • Proprietary Name: Lymph-Tone III
  • Non Proprietary Name: Adenosinum cyclophosphoricum, Arnica, Boldo, Calc iod, Calendula, Cartilago suis, Ceanothus, Coenzyme A, Echinacea, Hamamelis, Hepar sulph calc, Hypothalamus, Nadidum, Naja, Nat sulphuricum, Phaseolus, Phos, Phytolacca, Pinus syl, Pituitarum posterium, Pyrogenium, Silicea, Sulphur, Thuja occ, Thyroidinum, Viscum
  • Active Ingredient(s): 12 [hp_X]/59.1mL ADENOSINE CYCLIC PHOSPHATE; 12 [hp_X]/59.1mL ARNICA MONTANA WHOLE; 12 [hp_X]/59.1mL BOS TAURUS HYPOTHALAMUS; 12 [hp_X]/59.1mL CALCIUM IODIDE; 12 [hp_X]/59.1mL CALCIUM SULFIDE; 30 [hp_X]/59.1mL CALENDULA OFFICINALIS FLOWERING TOP; 9 [hp_X]/59.1mL CEANOTHUS AMERICANUS LEAF; 12 [hp_X]/59.1mL COENZYME A; 4 [hp_X]/59.1mL ECHINACEA ANGUSTIFOLIA; 12 [hp_X]/59.1mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; 12 [hp_X]/59.1mL HERRING SPERM DNA; 4 [hp_X]/59.1mL KIDNEY BEAN; 12 [hp_X]/59.1mL NADIDE; 15 [hp_X]/59.1mL NAJA NAJA VENOM; 4 [hp_X]/59.1mL PEUMUS BOLDUS LEAF; 15 [hp_X]/59.1mL PHOSPHORUS; 4 [hp_X]/59.1mL PHYTOLACCA AMERICANA ROOT; 9 [hp_X]/59.1mL PINUS SYLVESTRIS LEAFY TWIG; 12 [hp_X]/59.1mL RANCID BEEF; 12 [hp_X]/59.1mL SILICON DIOXIDE; 30 [hp_X]/59.1mL SODIUM SULFATE; 15 [hp_X]/59.1mL SULFUR; 6 [hp_X]/59.1mL SUS SCROFA CARTILAGE; 12 [hp_X]/59.1mL SUS SCROFA PITUITARY GLAND, POSTERIOR; 15 [hp_X]/59.1mL THUJA OCCIDENTALIS LEAFY TWIG; 9 [hp_X]/59.1mL THYROID, UNSPECIFIED; 12 [hp_X]/59.1mL VISCUM ALBUM FRUITING TOP
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Blood Coagulation Factor [EPC]; Calcium [CS]; Cations; Divalent [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Plant Proteins [CS]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Energetix Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/1/2017

Package Information

No. Package Code Package Description Billing Unit
164578-0172-159.1 mL in 1 BOTTLE (64578-0172-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0172The 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 NAMELymph-Tone IIIThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAdenosinum cyclophosphoricum, Arnica, Boldo, Calc iod, Calendula, Cartilago suis, Ceanothus, Coenzyme A, Echinacea, Hamamelis, Hepar sulph calc, Hypothalamus, Nadidum, Naja, Nat sulphuricum, Phaseolus, Phos, Phytolacca, Pinus syl, Pituitarum posterium, Pyrogenium, Silicea, Sulphur, Thuja occ, Thyroidinum, ViscumThe 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 DATE9/1/2017This 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 NAMEEnergetix CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEADENOSINE CYCLIC PHOSPHATE; ARNICA MONTANA WHOLE; BOS TAURUS HYPOTHALAMUS; CALCIUM IODIDE; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; CEANOTHUS AMERICANUS LEAF; COENZYME A; ECHINACEA ANGUSTIFOLIA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HERRING SPERM DNA; KIDNEY BEAN; NADIDE; NAJA NAJA VENOM; PEUMUS BOLDUS LEAF; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS LEAFY TWIG; RANCID BEEF; SILICON DIOXIDE; SODIUM SULFATE; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA PITUITARY GLAND, POSTERIOR; THUJA OCCIDENTALIS LEAFY TWIG; THYROID, UNSPECIFIED; VISCUM ALBUM FRUITING TOPAn 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 STRENGTH12; 12; 12; 12; 12; 30; 9; 12; 4; 12; 12; 4; 12; 15; 4; 15; 4; 9; 12; 12; 30; 15; 6; 12; 15; 9; 12 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL 
PHARM CLASSESAllergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Plant Proteins [CS], Vegetable Proteins [CS] 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 7/4/2025

Previous Code
Next Code