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: ADENOSINUM TRIPHOSPHORICUM DINATRUM, BRYONIA (ALBA), CEDRON, DIM (3, 3-DIINDOLYMETHANE), EQUOL, FAECALIS (ALKALIGENES), IGNATIA AMARA, LACHESIS MUTUS, PETROSELINUM SATIVUM, SANGUINARIA CANADENSIS, SEPIA, STANNUM METALLICUM, SULPHUR
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 649d19e2-3bed-4d2e-834d-4354a90d87e6
SPL ID: eae8a36a-2c73-47a6-9b31-e81cff8b61dc
Version: 1
Effective date: 2024-08-14
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:13

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		ADENOSINUM TRIPHOSPHORICUM DINATRUM, BRYONIA (ALBA), CEDRON, DIM (3, 3-DIINDOLYMETHANE), EQUOL, FAECALIS (ALKALIGENES), IGNATIA AMARA, LACHESIS MUTUS, PETROSELINUM SATIVUM, SANGUINARIA CANADENSIS, SEPIA, STANNUM METALLICUM, SULPHUR	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-2184-1	openfda.package_ndc
ndc	product	43742-2184	openfda.product_ndc
ndc11	package	43742218401	derived:openfda.package_ndc
spl id		eae8a36a-2c73-47a6-9b31-e81cff8b61dc	id
spl set id		649d19e2-3bed-4d2e-834d-4354a90d87e6	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: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: 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.