43742-1248 NDC - ADRENAL SUPPORT (ARALIA QUINQUEFOLIA, HUMULUS LUPULUS, ADRENALINUM, CORTISONE ACETICUM, SELENIUM METALLICUM, THYROIDINUM (SUIS), ARSENICUM ALBUM, CALCAREA CARBONICA, CONVALLARIA MAJALIS, CROTALUS HORRIDUS, FERRUM METALLICUM, NUX VOMICA, PHOSPHORUS, SEPIA, PHOSPHORICUM ACIDUM)

Drug Information

  • Product NDC: 43742-1248
  • Proprietary Name: Adrenal Support
  • Non Proprietary Name: Aralia Quinquefolia, Humulus Lupulus, Adrenalinum, Cortisone Aceticum, Selenium Metallicum, Thyroidinum (Suis), Arsenicum Album, Calcarea Carbonica, Convallaria Majalis, Crotalus Horridus, Ferrum Metallicum, Nux Vomica, Phosphorus, Sepia, Phosphoricum Acidum
  • Active Ingredient(s): 3 [hp_X]/mL AMERICAN GINSENG; 12 [hp_X]/mL ARSENIC TRIOXIDE; 12 [hp_X]/mL CONVALLARIA MAJALIS; 8 [hp_X]/mL CORTISONE ACETATE; 12 [hp_X]/mL CROTALUS HORRIDUS HORRIDUS VENOM; 8 [hp_X]/mL EPINEPHRINE; 3 [hp_X]/mL HOPS; 12 [hp_X]/mL IRON; 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 30 [hp_X]/mL PHOSPHORIC ACID; 12 [hp_X]/mL PHOSPHORUS; 8 [hp_X]/mL SELENIUM; 12 [hp_X]/mL SEPIA OFFICINALIS JUICE; 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 8 [hp_X]/mL THYROID
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Allergens [CS]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Dietary Proteins [CS]; Food Additives [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Plant Proteins [CS]; Seed Storage Proteins [CS]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/14/2018

Package Information

No. Package Code Package Description Billing Unit
143742-1248-160 mL in 1 BOTTLE, DROPPER (43742-1248-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1248The 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 NAMEAdrenal SupportThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAralia Quinquefolia, Humulus Lupulus, Adrenalinum, Cortisone Aceticum, Selenium Metallicum, Thyroidinum (Suis), Arsenicum Album, Calcarea Carbonica, Convallaria Majalis, Crotalus Horridus, Ferrum Metallicum, Nux Vomica, Phosphorus, Sepia, Phosphoricum AcidumThe 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 DATE9/14/2018This 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 Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMERICAN GINSENG; ARSENIC TRIOXIDE; CONVALLARIA MAJALIS; CORTISONE ACETATE; CROTALUS HORRIDUS HORRIDUS VENOM; EPINEPHRINE; HOPS; IRON; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORIC ACID; PHOSPHORUS; SELENIUM; SEPIA OFFICINALIS JUICE; STRYCHNOS NUX-VOMICA SEED; THYROIDAn 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 STRENGTH3; 12; 12; 8; 12; 8; 3; 12; 12; 30; 12; 8; 12; 12; 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 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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

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