Libidotone

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: Libidotone
Generic name: ARALIA QUINQUEFOLIA, BERBERIS VULGARIS, AGNUS CASTUS, AVENA SATIVA, CAUSTICUM, CONIUM MACULATUM, DAMIANA, GRAPHITES, HYPOPHYSIS SUIS, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SELENIUM METALLICUM, SEPIA
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4ceacaa0-0219-421a-8fff-c1784c3d0f70
SPL ID: 02da37af-eedc-4550-9641-2dbd4c359259
Version: 1
Effective date: 2026-02-27
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:18

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Libidotone	openfda.brand_name
generic name		ARALIA QUINQUEFOLIA, BERBERIS VULGARIS, AGNUS CASTUS, AVENA SATIVA, CAUSTICUM, CONIUM MACULATUM, DAMIANA, GRAPHITES, HYPOPHYSIS SUIS, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SELENIUM METALLICUM, SEPIA	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0741-1	openfda.package_ndc
ndc	product	44911-0741	openfda.product_ndc
ndc11	package	44911074101	derived:openfda.package_ndc
spl id		02da37af-eedc-4550-9641-2dbd4c359259	id
spl set id		4ceacaa0-0219-421a-8fff-c1784c3d0f70	set_id
unii		27YLU75U4W	openfda.unii
unii		DD5FO1WKFU	openfda.unii
unii		8W75VCV53Q	openfda.unii
unii		4QQN74LH4O	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		L0PFEMQ1DT	openfda.unii
unii		433OSF3U8A	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		MA9CQJ3F7F	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		RQ2CFA7WWJ	openfda.unii
unii		C88X29Y479	openfda.unii
unii		H6241UJ22B	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, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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