43742-1299 NDC - HGH VITALITY (AGNUS CASTUS, AMBRA GRISEA, APIOLUM, ESTRADIOL, ESTRIOL, L-DOPA, MELATONIN, TESTOSTERONE, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-LIPOICUM ACIDUM, NADIDUM, PANTOTHENIC ACID, SARCOLACTICUM ACIDUM, UBIDECARENONUM, BARYTA CARBONICA, CONIUM MACULATUM, SELENIUM METALLICUM, FOLLICULINUM, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HYPOTHALAMUS (SUIS), LYMPH NODE (SUIS), MEDULLA OSSIS SUIS, OOPHORINUM (SUIS), ORCHITINUM (SUIS), PANCREAS SUIS, SPLEEN (SUIS), HUMAN GROWTH HORMONE, PROTEUS)

Drug Information

Product NDC: 43742-1299

Proprietary Name: HGH Vitality

Non Proprietary Name: Agnus Castus, Ambra Grisea, Apiolum, Estradiol, Estriol, L-Dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, alpha-Lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Conium Maculatum, Selenium Metallicum, Folliculinum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (Suis), Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis), Orchitinum (Suis), Pancreas Suis, Spleen (Suis), Human Growth Hormone, Proteus

Active Ingredient(s):
  • 6 [hp_X]/1 CHASTE TREE;
  • 6 [hp_X]/1 AMBERGRIS;
  • 6 [hp_X]/1 APIOLE (PARSLEY);
  • 6 [hp_X]/1 ESTRADIOL;
  • 6 [hp_X]/1 ESTRIOL;
  • 6 [hp_X]/1 LEVODOPA;
  • 6 [hp_X]/1 MELATONIN;
  • 6 [hp_X]/1 TESTOSTERONE;
  • 8 [hp_X]/1 ADENOSINE TRIPHOSPHATE DISODIUM;
  • 8 [hp_X]/1 .ALPHA.-LIPOIC ACID;
  • 8 [hp_X]/1 NADIDE;
  • 8 [hp_X]/1 PANTOTHENIC ACID;
  • 8 [hp_X]/1 LACTIC ACID, L-;
  • 8 [hp_X]/1 UBIDECARENONE;
  • 8 [hp_X]/1 BARIUM CARBONATE;
  • 8 [hp_X]/1 CONIUM MACULATUM FLOWERING TOP;
  • 8 [hp_X]/1 SELENIUM;
  • 8 [hp_X]/1 ESTRONE;
  • 30 [hp_X]/1 SUS SCROFA UMBILICAL CORD;
  • 30 [hp_X]/1 SUS SCROFA ADRENAL GLAND;
  • 30 [hp_X]/1 PORK LIVER;
  • 30 [hp_X]/1 SUS SCROFA HYPOTHALAMUS;
  • 30 [hp_X]/1 SUS SCROFA LYMPH;
  • 30 [hp_X]/1 SUS SCROFA BONE MARROW;
  • 30 [hp_X]/1 SUS SCROFA OVARY;
  • 30 [hp_X]/1 SUS SCROFA TESTICLE;
  • 30 [hp_X]/1 SUS SCROFA PANCREAS;
  • 30 [hp_X]/1 SUS SCROFA SPLEEN;
  • 30 [hp_X]/1 SOMATROPIN;
  • 30 [hp_C]/1 PROTEUS MORGANII


Administration Route(s): ORAL

Dosage Form(s): TABLET

Labeler Information

Labeler Name: Deseret Biologicals
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/14/2019

Package Information

No. Package Code Package Description Billing Unit
143742-1299-190 TABLET in 1 BOTTLE (43742-1299-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1299The 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 NAMEHGH VitalityThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAgnus Castus, Ambra Grisea, Apiolum, Estradiol, Estriol, L-Dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, alpha-Lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Conium Maculatum, Selenium Metallicum, Folliculinum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (Suis), Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis), Orchitinum (Suis), Pancreas Suis, Spleen (Suis), Human Growth Hormone, ProteusThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe 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 DATE3/14/2019This 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 NAMEDeseret BiologicalsName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECHASTE TREE; AMBERGRIS; APIOLE (PARSLEY); ESTRADIOL; ESTRIOL; LEVODOPA; MELATONIN; TESTOSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; .ALPHA.-LIPOIC ACID; NADIDE; PANTOTHENIC ACID; LACTIC ACID, L-; UBIDECARENONE; BARIUM CARBONATE; CONIUM MACULATUM FLOWERING TOP; SELENIUM; ESTRONE; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA BONE MARROW; SUS SCROFA OVARY; SUS SCROFA TESTICLE; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SOMATROPIN; PROTEUS MORGANIIThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1 

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This page was last updated on: 12/20/2019