43742-2546 NDC - MALE SUPPORT (AGNUS CASTUS, AURUM METALLICUM, BENZOICUM ACIDUM, BRYONIA (ALBA), BUFO RANA, CALADIUM SEGUINUM, CHIMAPHILA UMBELLATA, CLEMATIS ERECTA, CONIUM MACULATUM, CORTISONE ACETICUM, HYPOTHALAMUS SUIS, KALI ARSENICOSUM, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PROSTATE (SUIS), RHODODENDRON CHRYSANTHUM, SABAL SERRULATA, SELENIUM METALLICUM, SEPIA, TESTOSTERONE, THUJA OCCIDENTALIS)

Drug Information

Product NDC: 43742-2546
Proprietary Name: Male Support
Non Proprietary Name: Agnus Castus, Aurum Metallicum, Benzoicum Acidum, Bryonia (Alba), Bufo Rana, Caladium Seguinum, Chimaphila Umbellata, Clematis Erecta, Conium Maculatum, Cortisone Aceticum, Hypothalamus Suis, Kali Arsenicosum, Lycopodium Clavatum, Natrum Muriaticum, Prostate (Suis), Rhododendron Chrysanthum, Sabal Serrulata, Selenium Metallicum, Sepia, Testosterone, Thuja Occidentalis
Active Ingredient(s): 6 [hp_X]/mL BENZOIC ACID; 12 [hp_X]/mL BRYONIA ALBA ROOT; 16 [hp_X]/mL BUFO BUFO CUTANEOUS GLAND; 12 [hp_X]/mL CHASTE TREE FRUIT; 6 [hp_X]/mL CHIMAPHILA UMBELLATA WHOLE; 6 [hp_X]/mL CLEMATIS RECTA FLOWERING TOP; 12 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP; 8 [hp_X]/mL CORTISONE ACETATE; 6 [hp_X]/mL DIEFFENBACHIA SEGUINE WHOLE; 12 [hp_X]/mL GOLD; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 15 [hp_X]/mL POTASSIUM ARSENITE ANHYDROUS; 6 [hp_X]/mL RHODODENDRON AUREUM LEAF; 6 [hp_X]/mL SAW PALMETTO; 12 [hp_X]/mL SELENIUM; 12 [hp_X]/mL SEPIA OFFICINALIS JUICE; 6 [hp_X]/mL SODIUM CHLORIDE; 8 [hp_X]/mL SUS SCROFA HYPOTHALAMUS; 8 [hp_X]/mL SUS SCROFA PROSTATE; 8 [hp_X]/mL TESTOSTERONE; 12 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): Allergens [CS]; Ammonium Ion Binding Activity [MoA]; Androgen Receptor Agonists [MoA]; Androgen [EPC]; Androstanes [CS]; Cell-mediated Immunity [PE]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Increased Histamine Release [PE]; Nitrogen Binding Agent [EPC]; Standardized Chemical Allergen [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:	6/15/2026
DEA Schedule:	CIII

Package Information

No.	Package Code	Package Description	Billing Unit

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	43742-2546	The 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 NAME	HUMAN OTC DRUG	Indicates 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 NAME	Male Support	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	Agnus Castus, Aurum Metallicum, Benzoicum Acidum, Bryonia (Alba), Bufo Rana, Caladium Seguinum, Chimaphila Umbellata, Clematis Erecta, Conium Maculatum, Cortisone Aceticum, Hypothalamus Suis, Kali Arsenicosum, Lycopodium Clavatum, Natrum Muriaticum, Prostate (Suis), Rhododendron Chrysanthum, Sabal Serrulata, Selenium Metallicum, Sepia, Testosterone, Thuja Occidentalis	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	LIQUID	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	6/15/2026	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	Product 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 NAME	Deseret Biologicals, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	BENZOIC ACID; BRYONIA ALBA ROOT; BUFO BUFO CUTANEOUS GLAND; CHASTE TREE FRUIT; CHIMAPHILA UMBELLATA WHOLE; CLEMATIS RECTA FLOWERING TOP; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; DIEFFENBACHIA SEGUINE WHOLE; GOLD; LYCOPODIUM CLAVATUM SPORE; POTASSIUM ARSENITE ANHYDROUS; RHODODENDRON AUREUM LEAF; SAW PALMETTO; SELENIUM; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PROSTATE; TESTOSTERONE; THUJA OCCIDENTALIS LEAFY TWIG	An 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 STRENGTH	6; 12; 16; 12; 6; 6; 12; 8; 6; 12; 12; 15; 6; 6; 12; 12; 6; 8; 8; 8; 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
PHARM CLASSES	Allergens [CS], Ammonium Ion Binding Activity [MoA], Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Histamine Release [PE], Nitrogen Binding Agent [EPC], Standardized Chemical Allergen [EPC]
DEA SCHEDULE	CIII	This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

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