Menopause

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:28:35

Label at a glance#

ProductMenopause HP
Active ingredientATROPA BELLADONNA, LACHESIS MUTA VENOM, MANGANESE ACETATE TETRAHYDRATE, STRYCHNOS NUX-VOMICA SEED, PULSATILLA PRATENSIS WHOLE, CLAVICEPS PURPUREA SCLEROTIUM, SEPIA OFFICINALIS JUICE, USTILAGO MAYDIS
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 12.50% of Belladonna 30X, Lachesis Mutus 30X, Manganum Aceticum 30X, Nux Vomica 30X, Pulsatilla (Pratensis) 30X, Secale Cornutum 30X, Sepia 30X, Ustilago Maidis 30X.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms due to autonomic dysregulation, dryness and irritation of the vagina.**

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

WARNINGS:

WARNINGS SECTION

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

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

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms due to autonomic dysregulation, dryness and irritation of the vagina.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
MENOPAUSE HP
1 fl. oz. (30 ml)

Menopause HPMenopause HP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0248-12024-10-29C16284748780-1ba0f9c33-14a0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0248-12024-01-30C16284748780-1ba0f9c33-14a0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0248-12022-03-10C16284748780-1ba0f9c33-14a0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0248-12021-01-29C16284748780-1ba0f9c33-14a0-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0248-1MenopauseHP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0248MENOPAUSE HP (BELLADONNA, LACHESIS MUTUS, MANGANUM ACETICUM, NUX VOMICA, PULSATILLA (PRATENSIS), SECALE CORNUTUM, SEPIA, USTILAGO MAIDIS) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20241031_6412a5f1-5587-4d4e-8d3f-692979415436.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
CLAVICEPS PURPUREA SCLEROTIUMACTIVE INGREDIENT01G9XEA93N1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
MANGANESE ACETATE TETRAHYDRATEACTIVE INGREDIENT9TO51D176N1
PULSATILLA PRATENSISACTIVE INGREDIENT8E272251DI1
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C21
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
USTILAGO MAYDISACTIVE INGREDIENT4K7Z7K7SWG1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
CLAVICEPS PURPUREA SCLEROTIUMACTIVE MOIETY01G9XEA93N1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
MANGANESE CATION (2+)ACTIVE MOIETYH6EP7W54571
PULSATILLA PRATENSISACTIVE MOIETY8E272251DI1
SEPIA OFFICINALIS JUICEACTIVE MOIETYQDL83WN8C21
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
USTILAGO MAYDISACTIVE MOIETY4K7Z7K7SWG1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
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
44911-024844911-0248-1

Ingredients#

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

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

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 · 2 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
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
Menopause HPBELLADONNA, LACHESIS MUTUS, MANGANUM ACETICUM, NUX VOMICA, PULSATILLA (PRATENSIS), SECALE CORNUTUM, SEPIA, USTILAGO MAIDISEnergique, Inc.6412a5f1-5587-4d4e-8d3f-6929794154362024-10-29WarningsExact identifier
ndc (package): 44911-0248-1
ndc (product): 44911-0248
ndc11 (package): 44911024801
spl id: 43f78cc7-08b2-4be9-96fb-8b86e3a840a0
spl set id: 6412a5f1-5587-4d4e-8d3f-692979415436

Reported adverse events (FAERS/openFDA)#

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