Sprayology Man Power

Manufacturer
Eight and Company
Effective date
2016-07-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:06

Label at a glance#

ProductSprayology Man Power
Active ingredientCHASTE TREE, AMERICAN GINSENG, SILVER NITRATE, ARNICA MONTANA, DIEFFENBACHIA SEGUINE, TURNERA DIFFUSA LEAFY TWIG, LACTUCA VIROSA, NUPHAR LUTEUM ROOT, SUS SCROFA TESTICLE, PHOSPHORIC ACID
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: ​Agnus castus 3X, Aralia quinquefolia 2X, Argentum nitricum 30C, Arnica Montana 3X, Caladium seginum 6X, Damiana 2X, Lactuca virosa 3X, Nuphar Luteum 2X, Orchitinum 6X, Phosphoricum acidum 200C.

WARNINGS SECTION

Warnings: If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • For adult men only. 2 sprays into the mouth 3 times per day.

OTC - PURPOSE SECTION

Temporarily relieves the symptoms of low male energy, including:

  • decreased sexual desire and vitality
  • muscular weakness
  • irritability
  • "the blues"

OTHER SAFETY INFORMATION

Other Information: Do not use if the transparent seal around spray bottle is broken or missing.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Glycerin 10% v/v, non-GMO organic alcohol 9% v/v and purified water.

INDICATIONS & USAGE SECTION

Temporarily relieves the symptoms of low male energy, including:

° decreased sexual desire and vitality

° muscular weakness

° irritability

° "the blues"

° natural

° gluten free

° no artificial flavors or colors

° no known negative side effects

° no known negative drug interactions

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61096-1025-12020-01-31C16284748780-19d75b9d0-164e-f424-e053-dadaa90a57ceSprayology Man Power

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61096-1025-1Sprayology Man Power41 mL in 1 BOTTLE, SPRAYLIQUID411
61096-1025-1Sprayology Man Power1 in 1 CARTONLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61096-1025SPRAYOLOGY MAN POWER (AGNUS CASTUS, ARALIA QUINQUEFOLIA, ARGENTUM NITRICUM, ARNICA MONTANA, CALADIUM SEGINUM, DAMIANA, LACTUCA VIROSA, NUPHAR LUTEUM, ORCHITINUM, PHOSPHORICUM ACIDUM) LIQUID [EIGHT AND COMPANY]1Legacy NDC, 2 package rows20160729_84d2c9bf-f57a-4dba-b93d-a08b240f4e79.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61096-102561096-1025-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML · Source PDF

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
1db5d427-edfa-4c8a-a15b-3b0bc58eba7084d2c9bf-f57a-4dba-b93d-a08b240f4e792016-07-29WarningsExact identifier
spl id: 1db5d427-edfa-4c8a-a15b-3b0bc58eba70
spl set id: 84d2c9bf-f57a-4dba-b93d-a08b240f4e79

Reported adverse events (FAERS/openFDA)#

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