Libidotone

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:37:45

Label at a glance#

ProductLibidotone
Active ingredientAMERICAN GINSENG, BERBERIS VULGARIS ROOT BARK, CHASTE TREE FRUIT, AVENA SATIVA FLOWERING TOP, CAUSTICUM, CONIUM MACULATUM FLOWERING TOP, TURNERA DIFFUSA LEAFY TWIG, GRAPHITE, SUS SCROFA PITUITARY GLAND, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, PHOSPHORIC ACID, PHOSPHORUS, SELENIUM, SEPIA OFFICINALIS JUICE
Label structure9 sections

Indications and uses

May temporarily relieve symptoms such as decreased sexual desire and feelings of fatigue.** **Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

Dosage and administration

Adults only: 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. 

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 7.13% of Agnus Castus 6X, Avena Sativa 6X, Causticum 12X, Conium Maculatum 12X, Damiana 12X, Graphites 12X, Hypophysis Suis 12X, Lachesis Mutus 12X, Lycopodium Clavatum 12X, Natrum Muriaticum 12X, Phosphoricum Acidum 12X, Phosphorus 12X, Selenium Metallicum 12X, Sepia 12X; 0.10% Aralia Quinquefolia 3X, Berberis Vulgaris 3X.

PURPOSE:

OTC - PURPOSE SECTION

May temporarily relieve symptoms such as decreased sexual desire and feelings of fatigue.**

**Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults only: 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional.

If symptoms persist for more than 7 days, consult your health care professional. 

USES:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms such as decreased sexual desire and feelings of fatigue.**

**Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579

800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

LIBIDOTONE

1 fl. oz. (30 ml)

LIBIDOTONELIBIDOTONE

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130363113700695GTIN-13: 0363113700695
EAN-13: 0363113700695
GTIN-12: 363113700695
UPC-A: 363113700695
GTIN storage (14 digits): 00363113700695
ENRG0829 Libidotone 04-17-15-.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0741-1Libidotone30 mL in 1 BOTTLE, DISPENSINGLIQUID301

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-074144911-0741-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LibidotoneARALIA 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, SEPIAEnergique, Inc.4ceacaa0-0219-421a-8fff-c1784c3d0f702026-02-27WarningsExact identifier
ndc (package): 44911-0741-1
ndc (product): 44911-0741
ndc11 (package): 44911074101
spl id: 02da37af-eedc-4550-9641-2dbd4c359259
spl set id: 4ceacaa0-0219-421a-8fff-c1784c3d0f70

Reported adverse events (FAERS/openFDA)#

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