FDA.reportPublic FDA data

Sprayology MenoPower

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 MenoPower
Active ingredientARNICA MONTANA, NITROGLYCERIN, LACHESIS MUTA VENOM, SUS SCROFA OVARY, SAGE, SANGUINARIA CANADENSIS ROOT, SEPIA OFFICINALIS JUICE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Arnica montana 200C, Glonoinum 200C, Lachesis mutus 200C, Oophorinum 30C, Salvia officinalis 2X, Sanguinaria canadensis 200C, Sepia 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 women only. 2 sprays into the mouth 3 times per day.

OTC - PURPOSE SECTION

Temporarily relieves common menopausal symptoms associated with hormonal imbalances, including:

  • emotional fluctuations
  • hot flashes and night sweats
  • irritability
  • vaginal dryness

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 purified water.

INDICATIONS & USAGE SECTION

Temporarily relieves common menopausal symptoms associated with hormonal imbalances, including:

° emotional fluctuations

° hot flashes and night sweats

° irritability

° vaginal dryness

° 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
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61096-1014-12020-01-31C16284748780-19d75b9d0-9a6f-f424-e053-dadaa90a57ceSprayology MenoPower

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61096-1014-1Sprayology MenoPower1 in 1 CARTONLIQUID11
61096-1014-1Sprayology MenoPower41 mL in 1 BOTTLE, SPRAYLIQUID411

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61096-1014SPRAYOLOGY MENOPOWER (ARNICA MONTANA, GLONOINUM, LACHESIS MUTUS, OOPHORINUM, SALVIA OFFICINALIS, SANGUINARIA CANADENSIS, SEPIA) LIQUID [EIGHT AND COMPANY]1Legacy NDC, 2 package rows20160729_cf1d6627-e327-4c43-944f-35b8ef8b2518.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61096-101461096-1014-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARNICA MONTANAO80TY208ZWACTIB
NITROGLYCERING59M7S0WS3ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
SUS SCROFA OVARYS7YTV04R8OACTIB
SAGE065C5D077JACTIB
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

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
a4cc117a-d62c-4047-b5b1-910dca49ca94cf1d6627-e327-4c43-944f-35b8ef8b25182016-07-29WarningsExact identifier
spl id: a4cc117a-d62c-4047-b5b1-910dca49ca94
spl set id: cf1d6627-e327-4c43-944f-35b8ef8b2518

Reported adverse events (FAERS/openFDA)#

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