FDA.reportPublic FDA data

MenoPower

Manufacturer
Eight and Company L.L.C | King Bio Inc. | Apotheca Company
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:36:18

Label at a glance#

ProductMenoPower
Active ingredientARNICA MONTANA WHOLE, NITROGLYCERIN, LACHESIS MUTA VENOM, SUS SCROFA OVARY, SAGE, SANGUINARIA CANADENSIS ROOT, SEPIA OFFICINALIS JUICE
Label structure10 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Arnica 200C, Glonoinum 200C, Lachesis 200C, Oophorinum 30C, Salvia 4X, Sanguinaria 200C, Sepia 200C

PURPOSE:

OTC - PURPOSE SECTION

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

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

WARNINGS:

WARNINGS SECTION

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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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

OTHER INFORMATION:

OTHER SAFETY INFORMATION

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

INDICATIONS:

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 & lactose free

° no artificial flavors or colors

° no known negative side effects

° no known negative drug interactions

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Non-GMO glycerin, v/v, organic alcohol 20% v/v and purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

Mfd. for Eight and Company L.L.C.

Gaithersburg, MD 20879 1.800.377.5787

www.sprayology.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 61096-2014-1

sprayology

Menopower

CONTROLS MENOPAUSE SYMPTOMS

HOMEOPATHIC ORAL SPRAY

1.38 fl.oz (41 ml)

Menopower LBLMenopower LBL

Menopower CTNMenopower CTN

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130361096001419GTIN-13: 0361096001419
EAN-13: 0361096001419
GTIN-12: 361096001419
UPC-A: 361096001419
GTIN storage (14 digits): 00361096001419		ETCO0012 MenoPower CTN.jpg

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
61096-2014-12023-12-14C16284748780-1ba0f9c33-4e83-a910-e053-dadaa90a0b85MenoPower
61096-2014-12023-01-30C16284748780-1ba0f9c33-4e83-a910-e053-dadaa90a0b85MenoPower
61096-2014-12021-02-15C16284748780-1ba0f9c33-4e83-a910-e053-dadaa90a0b85MenoPower
61096-2014-12021-01-29C16284748780-1ba0f9c33-4e83-a910-e053-dadaa90a0b85MenoPower

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61096-2014-1MenoPower1 in 1 CARTONLIQUID18
61096-2014-1MenoPower41 mL in 1 BOTTLE, SPRAYLIQUID418

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
NITROGLYCERINACTIVE INGREDIENTG59M7S0WS31
SAGEACTIVE INGREDIENT065C5D077J1
SANGUINARIA CANADENSIS ROOTACTIVE INGREDIENTN9288CD5081
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C21
SUS SCROFA OVARYACTIVE INGREDIENTS7YTV04R8O1
ARNICA MONTANAACTIVE MOIETYO80TY208ZW1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
NITROGLYCERINACTIVE MOIETYG59M7S0WS31
SAGEACTIVE MOIETY065C5D077J1
SANGUINARIA CANADENSIS ROOTACTIVE MOIETYN9288CD5081
SEPIA OFFICINALIS JUICEACTIVE MOIETYQDL83WN8C21
SUS SCROFA OVARYACTIVE MOIETYS7YTV04R8O1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61096-201461096-2014-1

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 MONTANA WHOLEO80TY208ZWACTIB
NITROGLYCERING59M7S0WS3ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
SUS SCROFA OVARYS7YTV04R8OACTIB
SAGE065C5D077JACTIB
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
MenoPowerARNICA, GLONOINUM, LACHESIS, OOPHORINUM, SALVIA, SANGUINARIA, SEPIAEight and Company L.L.C1e1e79fe-fa8f-4e05-bcff-3a792eb63b352025-12-18WarningsExact identifier
ndc (package): 61096-2014-1
ndc (product): 61096-2014
ndc11 (package): 61096201401
spl id: 8fdce44b-8097-4a66-85ec-139d23f0f264
spl set id: 1e1e79fe-fa8f-4e05-bcff-3a792eb63b35

Reported adverse events (FAERS/openFDA)#

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