55714-2565 NDC - THYROID-ADRENAL (ADRENALINUM, THYROIDINUM, ALOE, CALC. CARB., CHELIDONIUM MAJUS, CONIUM, GRAPHITES, IODIUM, LACHESIS, LYCOPODIUM, LYCOPUS VIRGINICUS, PHYTOLACCA, RHUS TOXICODENDRON, SILICEA, SPONGIA, ECHINACEA)

Drug Information

Product NDC: 55714-2565

Proprietary Name: Thyroid-Adrenal

Non Proprietary Name: Adrenalinum, Thyroidinum, Aloe, Calc. carb., Chelidonium majus, Conium, Graphites, Iodium, Lachesis, Lycopodium, Lycopus virginicus, Phytolacca, Rhus toxicodendron, Silicea, Spongia, Echinacea

Active Ingredient(s):
  • 15 [hp_X]/g ALOE;
  • 15 [hp_X]/g CHELIDONIUM MAJUS;
  • 15 [hp_X]/g CONIUM MACULATUM FLOWERING TOP;
  • 6 [hp_X]/g ECHINACEA, UNSPECIFIED;
  • 15 [hp_X]/g EPINEPHRINE;
  • 15 [hp_X]/g GRAPHITE;
  • 15 [hp_X]/g IODINE;
  • 15 [hp_X]/g LACHESIS MUTA VENOM;
  • 15 [hp_X]/g LYCOPODIUM CLAVATUM SPORE;
  • 15 [hp_X]/g LYCOPUS VIRGINICUS;
  • 15 [hp_X]/g OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 15 [hp_X]/g PHYTOLACCA AMERICANA ROOT;
  • 15 [hp_X]/g SILICON DIOXIDE;
  • 15 [hp_X]/g SPONGIA OFFICINALIS SKELETON, ROASTED;
  • 15 [hp_X]/g THYROID, UNSPECIFIED;
  • 15 [hp_X]/g TOXICODENDRON PUBESCENS LEAF


Administration Route(s): ORAL

Dosage Form(s): PELLET

Pharmacy Class(es):
  • Adrenergic alpha-Agonists [MoA];
  • Adrenergic beta-Agonists [MoA];
  • Catecholamine [EPC];
  • Catecholamines [CS];
  • alpha-Adrenergic Agonist [EPC];
  • beta-Adrenergic Agonist [EPC]

Labeler Information

Labeler Name: Newton Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/30/2020

Package Information

No. Package Code Package Description Billing Unit
155714-2565-128 g in 1 BOTTLE, GLASS (55714-2565-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55714-2565The 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 NAMEThyroid-AdrenalThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAdrenalinum, Thyroidinum, Aloe, Calc. carb., Chelidonium majus, Conium, Graphites, Iodium, Lachesis, Lycopodium, Lycopus virginicus, Phytolacca, Rhus toxicodendron, Silicea, Spongia, EchinaceaThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPELLETThe 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 DATE10/30/2020This 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 NAMENewton Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALOE; CHELIDONIUM MAJUS; CONIUM MACULATUM FLOWERING TOP; ECHINACEA, UNSPECIFIED; EPINEPHRINE; GRAPHITE; IODINE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; LYCOPUS VIRGINICUS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; SILICON DIOXIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; 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 STRENGTH15; 15; 15; 6; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15 
ACTIVE INGRED UNIT[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 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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This page was last updated on: 2/1/2023