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: CALTHA PALUSTRIS, CLEMATIS ERECTA, GALIUM APARINE, HEDERA HELIX, JUNIPERUS COMMUNIS, SEDUM ACRE, SEMPERVIVUM TECTORUM, THUJA OCCIDENTALIS, URTICA URENS, ECHINACEA (ANGUSTIFOLIA), ARGENTUM METALLICUM, CALCAREA FLUORICA, NITRICUM ACIDUM, PHOSPHORUS, CORTISONE ACETICUM, AURUM METALLICUM, APIS MELLIFICA, ONONIS SPINOSA, GAERTNER BACILLUS (BACH)
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1fcc1842-0ec7-4ec6-ac7f-6880ff5358c5
SPL ID: 5a1717ff-7c41-4f7b-ada7-45b5266f61fe
Version: 4
Effective date: 2024-08-15
Source export date: 2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:29:15

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		CALTHA PALUSTRIS, CLEMATIS ERECTA, GALIUM APARINE, HEDERA HELIX, JUNIPERUS COMMUNIS, SEDUM ACRE, SEMPERVIVUM TECTORUM, THUJA OCCIDENTALIS, URTICA URENS, ECHINACEA (ANGUSTIFOLIA), ARGENTUM METALLICUM, CALCAREA FLUORICA, NITRICUM ACIDUM, PHOSPHORUS, CORTISONE ACETICUM, AURUM METALLICUM, APIS MELLIFICA, ONONIS SPINOSA, GAERTNER BACILLUS (BACH)	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1602-1	openfda.package_ndc
ndc	product	43742-1602	openfda.product_ndc
ndc11	package	43742160201	derived:openfda.package_ndc
spl id		5a1717ff-7c41-4f7b-ada7-45b5266f61fe	id
spl set id		1fcc1842-0ec7-4ec6-ac7f-6880ff5358c5	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: Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "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.