HP Axis

Product NDC

43742-1514

11-digit product format

437421514

Labeler code

43742

Product ID

43742-1514_754c41aa-652d-4e5e-89a6-dae139ad2444

Type

HUMAN OTC DRUG

Nonproprietary name

Argentum Nitricum, Berberis Vulgaris, Iodium, Kali Carbonicum, Natrum Muriaticum, Adrenalinum, Cortisone Aceticum, DHEA, Glandula Suprarenalis Suis, Hypophysis Suis, Hypothalamus Suis, Melatonin, Testosterone, Arsenicum Album, Phosphorus, Proteus (Vulgaris), Sepia, Silicea, Alloxanum, Corticotropin Releasing Hormone, Adrenocorticotrophin, Aldosterone

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2019-07-26

Substance

ALDOSTERONE; ALLOXAN; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; CORTICORELIN; CORTICOTROPIN; CORTISONE ACETATE; EPINEPHRINE; IODINE; MELATONIN; PHOSPHORUS; POTASSIUM CARBONATE; PRASTERONE; PROTEUS VULGARIS; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SILVER NITRATE; SODIUM CHLORIDE; SUS SCROFA ADRENAL GLAND; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PITUITARY GLAND; TESTOSTERONE

Active strength

15; 18; 12; 6; 12; 15; 8; 8; 6; 8; 12; 6; 8; 12; 12; 12; 6; 6; 8; 8; 8; 8 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Pharmacologic classes

Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Catecholamine [EPC], Catecholamines [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes