FDA.reportPublic FDA data

MENOPAUSE HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:35:57

Label at a glance#

ProductMENOPAUSE HP
Active ingredientATROPA BELLADONNA, BLACK COHOSH, LACHESIS MUTA VENOM, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS, CLAVICEPS PURPUREA SCLEROTIUM, SEPIA OFFICINALIS JUICE, USTILAGO MAYDIS
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Belladonna 30C, Cimicifuga Racemosa 30C, Lachesis Mutus 30C, Nux Vomica 30C, Pulsatilla 30C, Secale Cornutum 30C, Sepia 30C, Ustilago Maidis 30X

INDICATIONS & USAGE SECTION

USES: Temporarily relieves symptoms associated with menopause, such as lower back pain, hot flashes.**

WARNINGS SECTION

WARNING:

*Consult a physician for us in children under 12 years of age.

* IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.

* KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

* Do not use if TAMPER EVIDENT seal is broken or missing.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults and children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

REFERENCES SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

OTC - QUESTIONS SECTION

QUESTIONS AND COMMENTS?

MFG FOR: Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

OTC - PURPOSE SECTION

USES: Temporarily relieves symptoms associated with menopause, such as lower back pain, hot flashes.**

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0030-1

MENOPAUSE HP

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

Image Of LabelImage Of Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730001924GTIN-13: 0877730001924
EAN-13: 0877730001924
GTIN-12: 877730001924
UPC-A: 877730001924
GTIN storage (14 digits): 00877730001924		MENOPAUSE HP.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0030-12023-01-19C16284748780-19855d018-eddd-cd31-e053-dbdaa90ab51aMENOPAUSE HP
43406-0030-12019-11-27C16284748780-19855d018-eddd-cd31-e053-dbdaa90ab51aMENOPAUSE HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0030-1MENOPAUSE HP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
BLACK COHOSHACTIVE INGREDIENTK73E24S6X91
CLAVICEPS PURPUREA SCLEROTIUMACTIVE INGREDIENT01G9XEA93N1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C21
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
USTILAGO MAYDISACTIVE INGREDIENT4K7Z7K7SWG1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
BLACK COHOSHACTIVE MOIETYK73E24S6X91
CLAVICEPS PURPUREA SCLEROTIUMACTIVE MOIETY01G9XEA93N1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
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 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-003043406-0030-1

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
ATROPA BELLADONNAWQZ3G9PF0HACTIB
BLACK COHOSHK73E24S6X9ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
CLAVICEPS PURPUREA SCLEROTIUM01G9XEA93NACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
USTILAGO MAYDIS4K7Z7K7SWGACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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 HPATROPA BELLADONNA, BLACK COHOSH, LACHESIS MUTA VENOM, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS, CLAVICEPS PURPUREA SCLEROTIUM, SEPIA OFFICINALIS JUICE, USTILAGO MAYDISNatural Creations, Inc.38798520-1fcd-4494-b7b7-058633879abf2025-12-16WarningsExact identifier
ndc (package): 43406-0030-1
ndc (product): 43406-0030
ndc11 (package): 43406003001
spl id: 7a9d5953-6d0e-4888-9642-dc149e4aa76a
spl set id: 38798520-1fcd-4494-b7b7-058633879abf

Reported adverse events (FAERS/openFDA)#

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