43742-1298 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,)

Drug Information

Product NDC: 43742-1298

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,

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


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Amino Acids;
  • Aromatic [CS];
  • Androgen Receptor Agonists [MoA];
  • Androgen [EPC];
  • Androstanes [CS];
  • Aromatic Amino Acid [EPC];
  • Estradiol Congeners [CS];
  • Estrogen Receptor Agonists [MoA];
  • Estrogen [EPC];
  • Human Growth Hormone [CS];
  • Recombinant Human Growth Hormone [EPC]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/27/2018
End Marketing Date:6/24/2024
DEA Schedule:CIII

Package Information

No. Package Code Package Description Billing Unit
143742-1298-130 mL in 1 BOTTLE, DROPPER (43742-1298-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1298The 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,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 DATE8/27/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE6/24/2024This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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 Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME.ALPHA.-LIPOIC ACID; ADENOSINE TRIPHOSPHATE DISODIUM; AMBERGRIS; APIOLE (PARSLEY); BARIUM CARBONATE; CHASTE TREE; ESTRADIOL; ESTRIOL; ESTRONE; LACTIC ACID, L-; LEVODOPA; MELATONIN; NADIDE; PANTOTHENIC ACID; PORK LIVER; PROTEUS MORGANII; SELENIUM; SOMATROPIN; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA OVARY; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SUS SCROFA TESTICLE; SUS SCROFA UMBILICAL CORD; TESTOSTERONE; UBIDECARENONEAn 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 STRENGTH8; 8; 6; 6; 8; 6; 6; 6; 8; 8; 6; 6; 8; 8; 30; 30; 8; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 6; 8 
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_C]/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 CLASSESAmino Acids, Aromatic [CS], Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Aromatic Amino Acid [EPC], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Human Growth Hormone [CS], Recombinant Human Growth Hormone [EPC] 
DEA SCHEDULECIIIThis is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

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