Home NDC 43742-1514 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 SILVER NITRATE; BERBERIS VULGARIS ROOT BARK; IODINE; POTASSIUM CARBONATE; SODIUM CHLORIDE; EPINEPHRINE; CORTISONE ACETATE; PRASTERONE; SUS SCROFA ADRENAL GLAND; SUS SCROFA PITUITARY GLAND; SUS SCROFA HYPOTHALAMUS; MELATONIN; TESTOSTERONE; ARSENIC TRIOXIDE; PHOSPHORUS; PROTEUS VULGARIS; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; ALLOXAN; CORTICORELIN; CORTICOTROPIN; ALDOSTERONE
Active strength 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 12; 12; 12; 12; 12; 18; 12; 15; 15 [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_C]/mL; [hp_C]/mL; [hp_C]/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 Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base HP Axis
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILVER NITRATE 6 [hp_X]/mL BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL IODINE 6 [hp_X]/mL POTASSIUM CARBONATE 6 [hp_X]/mL SODIUM CHLORIDE 6 [hp_X]/mL EPINEPHRINE 8 [hp_X]/mL CORTISONE ACETATE 8 [hp_X]/mL PRASTERONE 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL SUS SCROFA PITUITARY GLAND 8 [hp_X]/mL SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL MELATONIN 8 [hp_X]/mL TESTOSTERONE 8 [hp_X]/mL ARSENIC TRIOXIDE 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL PROTEUS VULGARIS 12 [hp_X]/mL SEPIA OFFICINALIS JUICE 12 [hp_X]/mL SILICON DIOXIDE 12 [hp_X]/mL ALLOXAN 18 [hp_X]/mL CORTICORELIN 12 [hp_C]/mL CORTICOTROPIN 15 [hp_C]/mL ALDOSTERONE 15 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 22 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-1514-1 HP Axis 30 mL in 1 BOTTLE, DROPPER LIQUID 30 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1514 HP AXIS (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) LIQUID [DESERET BIOLOGICALS, INC.] 7 Current NDC, Legacy NDC, 1 package rows 20240925_402f5b05-c71e-4dba-bc2b-049aee42952a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HP Axis 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 Deseret Biologicals, Inc. 402f5b05-c71e-4dba-bc2b-049aee42952a 2024-09-23 Warnings Exact identifier ndc (product): 43742-1514
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1514-1 43742151401 30 mL in 1 BOTTLE, DROPPER (43742-1514-1) 30 ml 2019-07-26 0000-00-00 No No Current