FDA.reportPublic FDA data

Menopause Relief

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2018-10-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:49:06

Label at a glance#

ProductMenopause Relief
Active ingredientSANGUINARIA CANADENSIS ROOT, STRYCHNOS IGNATII SEED, SEPIA OFFICINALIS JUICE, ADENOSINE TRIPHOSPHATE DISODIUM, BRYONIA ALBA ROOT, SIMABA CEDRON SEED, 3,3'-DIINDOLYLMETHANE, EQUOL, (-)-, SULFUR, APIOLE (PARSLEY), LACHESIS MUTA VENOM, TIN, ALCALIGENES FAECALIS
Label structure9 sections

Dosage and administration

Adults 3-10 drops under the tongue 3 times daily or as directed by your health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Sanguinaria Canadensis 3X, Ignatia Amara 4X, Sepia 4X, Adenosinum Triphosphoricum Dinatrum 6X, Bryonia (Alba) 6X, Cedron 6X, DIM (3,3’-Diindolymethane) 6X, Equol 6X, Sulphur 6X, Apiolum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Lachesis Mutus 12X, Stannum Metallicum 12X, Faecalis (Alkaligenes) 30C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to hormone fluctuations associated with menopause, including hot flashes, mood swings, night sweats, flushing, headache, weight gain, insomnia, weakness, and lack of energy.**

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

WARNINGS:

WARNINGS SECTION

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

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

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults 3-10 drops under the tongue 3 times daily or as directed by your health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to hormone fluctuations associated with menopause, including hot flashes, mood swings, night sweats, flushing, headache, weight gain, insomnia, weakness, and lack of energy.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By:  Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070     www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0824-1

HOMEOPATHIC

MENOPAUSE RELIEF

1 FL OZ (30 ml)

Menopause ReliefMenopause Relief

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-082443742-0824-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
ADENOSINE TRIPHOSPHATE DISODIUM5L51B4DR1GACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
SIMABA CEDRON SEEDKHI40967MVACTIB
3,3'-DIINDOLYLMETHANESSZ9HQT61ZACTIB
EQUOL, (-)-2T6D2HPX7QACTIB
SULFUR70FD1KFU70ACTIB
APIOLE (PARSLEY)QQ67504PXOACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
TIN387GMG9FH5ACTIB
ALCALIGENES FAECALIS05KB30NGW2ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
95c00d8d-0f42-42c9-89ff-4d015d141521afb7256f-909c-47cc-9a7d-feeba98c7ba12018-10-01WarningsExact identifier
spl id: 95c00d8d-0f42-42c9-89ff-4d015d141521
spl set id: afb7256f-909c-47cc-9a7d-feeba98c7ba1

Reported adverse events (FAERS/openFDA)#

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