Libido

Manufacturer
Newton Laboratories, Inc.
Effective date
2020-12-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:13:52

Label at a glance#

ProductLibido
Active ingredientBERBERIS VULGARIS ROOT BARK, CHASTE TREE FRUIT, AMERICAN GINSENG, BARIUM CARBONATE, BRYONIA ALBA ROOT, DIEFFENBACHIA SEGUINE, LYTTA VESICATORIA, CAUSTICUM, CHELIDONIUM MAJUS, CINCHONA OFFICINALIS BARK, CONIUM MACULATUM FLOWERING TOP, GAULTHERIA PROCUMBENS TOP, GRAPHITE, POTASSIUM CARBONATE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, ONOSMODIUM VIRGINIANUM, PHOSPHORUS, SAW PALMETTO, SELENIUM, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, DELPHINIUM STAPHISAGRIA SEED, GOLDENSEAL, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for associated symptoms such as decreased desire, dryness, impotence, anxiety and hypersexuality.

DOSAGE & ADMINISTRATION SECTION

Directions: Adults, take 6 drops by mout one to four times daily or as directed by a health professional.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Hydrastis canadensis 6x, Thuja occidentalis 6x, Agnus castus 15x, Aralia quinquefolia 15x, Baryta carbonica 15x, Berberis vulgaris 15x, Bryonia 15x, Caladium seguinum 15x, Cantharis 15x, Causticum 15x, Chelidonium majus 15x, Cinchona officinalis 15x, Conium maculatum 15x, Gaultheria procumbens 15x, Graphites 15x, Kali carbonicum 15x, Lycopodium clavatum 15x, Nux vomica 15x, Onosmodium virginianum 15x, Phosphorus 15x, Sabal serrulata 15x, Selenium metallicum 15x, Sepia 15x, Silicea 15x, Staphysagria 15x

OTC - PURPOSE SECTION

Formulated for associated symptoms such as decreased desire, dryness, impotence, anxiety and hypersexuality.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-4826-1Libido30 mL in 1 BOTTLE, GLASSLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-4826LIBIDO (AGNUS, ARALIA QUINQUEFOLIA, BARYTA CARB., BERBER. VULG., BRYONIA, CALADIUM SEGUINUM, CANTHARIS, CAUSTICUM, CHELIDONIUM MAJUS, CINCHONA, CONIUM, GAULTHERIA PROCUMBENS, GRAPHITES, KALI CARB., LYCOPODIUM, NUX VOM., ONOSMODIUM VIRGINIANUM, PHOSPHORUS, SABAL, SELENIUM, SEPIA, SILICEA, STAPHYSAG., HYDRASTIS, THUJA OCC) LIQUID [NEWTON LABORATORIES, INC.]2Legacy NDC, 1 package rows20201205_995db4fc-217b-cc09-e053-2a95a90a8329.zip

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-482655714-4826-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
b5a909c3-7ca5-ba64-e053-2a95a90a66b8995db4fc-217b-cc09-e053-2a95a90a83292020-12-04WarningsExact identifier
spl id: b5a909c3-7ca5-ba64-e053-2a95a90a66b8
spl set id: 995db4fc-217b-cc09-e053-2a95a90a8329

Reported adverse events (FAERS/openFDA)#

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