64578-0086 NDC - LYMPH-TONE (ADENOSINUM CYCLOPHOSPHORICUM, APIS MELLIFICA, ARANEA DIADEMA, BELLADONNA, BOLDO, CALCAREA CARBONICA, ECHINACEA (ANGUSTIFOLIA),GALIUM APARINE, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI IODATUM, PHOSPHORUS, PHYTOLACCA DECANDRA, PINUS SYLVESTRIS, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (VULGARIS), RHUS TOX, SCROPHULARIA NODOSA, SULPHUR, THYROIDINUM (BOVINE))

Drug Information

Product NDC: 64578-0086

Proprietary Name: Lymph-Tone

Non Proprietary Name: Adenosinum Cyclophosphoricum, Apis Mellifica, Aranea Diadema, Belladonna, Boldo, Calcarea Carbonica, Echinacea (Angustifolia),Galium Aparine, Glandula Suprarenalis Suis, Hypothalamus (Bovine), Kali Iodatum, Phosphorus, Phytolacca Decandra, Pinus Sylvestris, Pituitarum Posterium (Bovine), Pulsatilla (Vulgaris), Rhus Tox, Scrophularia Nodosa, Sulphur, Thyroidinum (Bovine)

Active Ingredient(s):
  • 12 [hp_X]/mL ADENOSINE CYCLIC PHOSPHATE;
  • 12 [hp_X]/mL APIS MELLIFERA;
  • 12 [hp_X]/mL ARANEUS DIADEMATUS;
  • 12 [hp_X]/mL ATROPA BELLADONNA;
  • 4 [hp_X]/mL PEUMUS BOLDUS LEAF;
  • 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 4 [hp_X]/mL ECHINACEA ANGUSTIFOLIA;
  • 12 [hp_X]/mL GALIUM APARINE;
  • 9 [hp_X]/mL SUS SCROFA ADRENAL GLAND;
  • 12 [hp_X]/mL BOS TAURUS HYPOTHALAMUS;
  • 4 [hp_X]/mL POTASSIUM IODIDE;
  • 12 [hp_X]/mL PHOSPHORUS;
  • 4 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 9 [hp_X]/mL PINUS SYLVESTRIS LEAFY TWIG;
  • 12 [hp_X]/mL BOS TAURUS PITUITARY GLAND;
  • 12 [hp_X]/mL PULSATILLA VULGARIS;
  • 12 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF;
  • 12 [hp_X]/mL SCROPHULARIA NODOSA;
  • 12 [hp_X]/mL SULFUR;
  • 12 [hp_X]/mL THYROID, PORCINE;
  • 12 [hp_X]/mL THYROID, BOVINE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Energetix Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/2/2015

Package Information

No. Package Code Package Description Billing Unit
164578-0086-159.1 mL in 1 BOTTLE, DROPPER (64578-0086-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0086The 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-ToneThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXIA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMEAdenosinum Cyclophosphoricum, Apis Mellifica, Aranea Diadema, Belladonna, Boldo, Calcarea Carbonica, Echinacea (Angustifolia),Galium Aparine, Glandula Suprarenalis Suis, Hypothalamus (Bovine), Kali Iodatum, Phosphorus, Phytolacca Decandra, Pinus Sylvestris, Pituitarum Posterium (Bovine), Pulsatilla (Vulgaris), Rhus Tox, Scrophularia Nodosa, Sulphur, 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 DATE7/2/2015This 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 CorpName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEADENOSINE CYCLIC PHOSPHATE; APIS MELLIFERA; ARANEUS DIADEMATUS; ATROPA BELLADONNA; PEUMUS BOLDUS LEAF; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ECHINACEA ANGUSTIFOLIA; GALIUM APARINE; SUS SCROFA ADRENAL GLAND; BOS TAURUS HYPOTHALAMUS; POTASSIUM IODIDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS LEAFY TWIG; BOS TAURUS PITUITARY GLAND; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; SCROPHULARIA NODOSA; SULFUR; THYROID, PORCINE; THYROID, BOVINEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 4; 12; 4; 12; 9; 12; 4; 12; 4; 9; 12; 12; 12; 12; 12; 12; 12 
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 

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This page was last updated on: 9/13/2019