Male Stimulant

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2018-10-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:48:04

Label at a glance#

ProductMale Stimulant
Active ingredientAMERICAN GINSENG, CHASTE TREE, ASCORBIC ACID, DIEFFENBACHIA SEGUINE, POTASSIUM BROMIDE, STRYCHNINE PHOSPHATE DIHYDRATE, LYTTA VESICATORIA, TURNERA DIFFUSA LEAFY TWIG, SUS SCROFA UMBILICAL CORD, SUS SCROFA ADRENAL GLAND, SUS SCROFA PITUITARY GLAND, SUS SCROFA TESTICLE, SUS SCROFA PROSTATE, CONIUM MACULATUM FLOWERING TOP, SUS SCROFA DIENCEPHALON, PORK HEART, FERROSOFERRIC PHOSPHATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SELENIUM, ZINC, SUS SCROFA PINEAL GLAND, CORTISONE ACETATE, MANGANESE PHOSPHATE, DIBASIC, LYCOPODIUM CLAVATUM SPORE, TESTOSTERONE, SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Aralia Quinquefolia 4X, Agnus Castus 6X, Ascorbicum Acidum 6X, Caladium Seguinum 6X, Kali Bromatum 6X, Strychninum Phosphoricum 6X, Cantharis 8X, Damiana 8X, Funiculus Umbilicalis Suis 8X, Glandula Suprarenalis Suis 8X, Hypophysis Suis 8X, Orchitinum (Suis) 8X, Prostate (Suis) 8X, Conium Maculatum 8X, 28X, Diencephalon (Suis) 8X, 30X, 200X, Heart (Suis) 8X, 30X, 200X, Ferrum Phosphoricum 10X, Magnesia Phosphorica 10X, Selenium Metallicum 10X, Zincum Metallicum 10X, Pineal Gland (Suis) 12X, 30X, 200X, Cortisone Aceticum 13X, Manganum Phosphoricum 20X, Lycopodium Clavatum 28X, Testosterone 30X, 60X, 200X, Morgan Gaertner 30C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

Temporary relief of symptoms related to male hormonal problems such as libido difficulties and fatigue.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact physician or a 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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

Temporary relief of symptoms related to male hormonal problems such as libido difficulties and fatigue.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070    www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO
NDC 43742-0772-1
HOMEOPATHIC
MALE
STIMULANT
1 FL OZ (30 ml)

Male StimulantMale Stimulant

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-077243742-0772-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
42bd1f3e-560f-4dda-b360-2a0457159b5a6d223bcb-b649-4881-928f-210c6d6d60022018-10-25WarningsExact identifier
spl id: 42bd1f3e-560f-4dda-b360-2a0457159b5a
spl set id: 6d223bcb-b649-4881-928f-210c6d6d6002

Reported adverse events (FAERS/openFDA)#

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