Bio Galium Phase

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: Bio Galium Phase
Generic name: APIS MELLIFICA, ARGENTUM METALLICUM, AURUM METALLICUM, CALCAREA FLUORICA, CALTHA PALUSTRIS, CLEMATIS ERECTA, CORTISONE ACETICUM, ECHINACEA (ANGUSTIFOLIA), GAERTNER BACILLUS (BACH), GALIUM APARINE, HEDERA HELIX, JUNIPERUS COMMUNIS, NITRICUM ACIDUM, ONONIS SPINOSA, PHOSPHORUS, SEDUM ACRE, SEMPERVIVUM TECTORUM, THUJA OCCIDENTALIS, URTICA URENS
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 902f38c5-b870-4313-9b0b-e69ca357d844
SPL ID: c35c1734-dc18-4c63-83b9-813bb66edbe8
Version: 2
Effective date: 2026-01-09
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:31

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Bio Galium Phase	openfda.brand_name
generic name		APIS MELLIFICA, ARGENTUM METALLICUM, AURUM METALLICUM, CALCAREA FLUORICA, CALTHA PALUSTRIS, CLEMATIS ERECTA, CORTISONE ACETICUM, ECHINACEA (ANGUSTIFOLIA), GAERTNER BACILLUS (BACH), GALIUM APARINE, HEDERA HELIX, JUNIPERUS COMMUNIS, NITRICUM ACIDUM, ONONIS SPINOSA, PHOSPHORUS, SEDUM ACRE, SEMPERVIVUM TECTORUM, THUJA OCCIDENTALIS, URTICA URENS	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-2202-1	openfda.package_ndc
ndc	product	43742-2202	openfda.product_ndc
ndc11	package	43742220201	derived:openfda.package_ndc
spl id		c35c1734-dc18-4c63-83b9-813bb66edbe8	id
spl set id		902f38c5-b870-4313-9b0b-e69ca357d844	set_id
unii		27YLU75U4W	openfda.unii
unii		3DGJ7BUA01	openfda.unii
unii		3M4G523W1G	openfda.unii
unii		O3B55K4YKI	openfda.unii
unii		883WKN7W8X	openfda.unii
unii		411VRN1TV4	openfda.unii
unii		1NT28V9397	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		RP8496915M	openfda.unii
unii		3D10KUA6BM	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		Y3V16D4PV4	openfda.unii
unii		2496VW6S9J	openfda.unii
unii		O84B5194RL	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		Z4B6561488	openfda.unii
unii		6S9317F2UT	openfda.unii
unii		396421SP9F	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.