Home FDA labels 2f80d111-fe7c-419f-8bbb-ef7dfb1017d6 Menopause 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
Generic name AGNUS CASTUS, ANGELICA SINENSIS RADIX, APIS MELLIFICA, ARALIA QUINQUEFOLIA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, GALIUM APARINE, GLYCYRRHIZA GLABRA, OOPHORINUM SUIS, SEPIA, THUJA OCCIDENTALIS, VISCUM ALBUM
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 3e17fa78-f5c2-47eb-9bb6-075ccffd01b6
SPL ID 2f80d111-fe7c-419f-8bbb-ef7dfb1017d6
Version 7
Effective date 2024-07-01
Source export date 2026-09-28
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:37:10 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Menopause openfda.brand_name generic name AGNUS CASTUS, ANGELICA SINENSIS RADIX, APIS MELLIFICA, ARALIA QUINQUEFOLIA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, GALIUM APARINE, GLYCYRRHIZA GLABRA, OOPHORINUM SUIS, SEPIA, THUJA OCCIDENTALIS, VISCUM ALBUM openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0092-2 openfda.package_ndc ndc package 50845-0092-1 openfda.package_ndc ndc product 50845-0092 openfda.product_ndc ndc11 package 50845009202 derived:openfda.package_ndc ndc11 package 50845009201 derived:openfda.package_ndc spl id 2f80d111-fe7c-419f-8bbb-ef7dfb1017d6 id spl set id 3e17fa78-f5c2-47eb-9bb6-075ccffd01b6 set_id unii 2788Z9758H openfda.unii unii 8W75VCV53Q openfda.unii unii O80TY208ZW openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii S7YTV04R8O openfda.unii unii 433OSF3U8A openfda.unii unii B66F4574UG openfda.unii unii BK9092J5MP openfda.unii unii 7S82P3R43Z openfda.unii unii Z4B6561488 openfda.unii unii K73E24S6X9 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a doctor before using product. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Other information. Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.