HP Axis

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: HP Axis
Generic 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
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 402f5b05-c71e-4dba-bc2b-049aee42952a
SPL ID: 754c41aa-652d-4e5e-89a6-dae139ad2444
Version: 7
Effective date: 2024-09-23
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:07:31

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 30 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		HP Axis	openfda.brand_name
generic 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	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1514-1	openfda.package_ndc
ndc	product	43742-1514	openfda.product_ndc
ndc11	package	43742151401	derived:openfda.package_ndc
spl id		754c41aa-652d-4e5e-89a6-dae139ad2444	id
spl set id		402f5b05-c71e-4dba-bc2b-049aee42952a	set_id
unii		27YLU75U4W	openfda.unii
unii		4964P6T9RB	openfda.unii
unii		459AG36T1B	openfda.unii
unii		883WKN7W8X	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		305OE8862Y	openfda.unii
unii		9679TC07X4	openfda.unii
unii		K0U68Q2TXA	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		L0PFEMQ1DT	openfda.unii
unii		3XMK78S47O	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		6SW5YHA5NG	openfda.unii
unii		11T9HCO30O	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		JL5DK93RCL	openfda.unii
unii		N6R0856Z79	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.