Menopause Relief

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Menopause Relief
Generic name: SANGUINARIA CANADENSIS, SEPIA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, DIM (3, 3-DIINDOLYMETHANE), EQUOL, SULPHUR, PETROSELINUM SATIVUM, BRYONIA (ALBA), IGNATIA AMARA, CEDRON, LACHESIS MUTUS, STANNUM METALLICUM, FAECALIS (ALKALIGENES)
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 802e3090-79fe-4daa-8b03-5843e33f6978
SPL ID: 6e465431-8fda-4058-9a98-4dc320d34733
Version: 4
Effective date: 2024-08-14
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:12:54

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Menopause Relief	openfda.brand_name
generic name		SANGUINARIA CANADENSIS, SEPIA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, DIM (3, 3-DIINDOLYMETHANE), EQUOL, SULPHUR, PETROSELINUM SATIVUM, BRYONIA (ALBA), IGNATIA AMARA, CEDRON, LACHESIS MUTUS, STANNUM METALLICUM, FAECALIS (ALKALIGENES)	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1590-1	openfda.package_ndc
ndc	product	43742-1590	openfda.product_ndc
ndc11	package	43742159001	derived:openfda.package_ndc
spl id		6e465431-8fda-4058-9a98-4dc320d34733	id
spl set id		802e3090-79fe-4daa-8b03-5843e33f6978	set_id
unii		387GMG9FH5	openfda.unii
unii		SSZ9HQT61Z	openfda.unii
unii		5L51B4DR1G	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		KHI40967MV	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		2T6D2HPX7Q	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		1WZA4Y92EX	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		05KB30NGW2	openfda.unii
unii		N9288CD508	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: Keep out of reach of children. In case of overdose, contact a physician or 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.

Reported adverse events (FAERS/openFDA)#

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