Home FDA labels b5aae85f-4c52-e3b4-e053-2995a90adb9b Mega Menses 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 Mega Menses
Generic name APIS MELLIFICA, HAMAMELIS VIRGINIANA, HYDRASTIS CANADENSIS, ALETRIS FARINOSA, APOCYNUM CANNABINUM, CINCHONA OFFICINALIS, CINNAMOMUM, CONIUM MACULATUM, HELONIAS DIOICA, LILIUM TIGRINUM, MILLEFOLIUM, PHOSPHORUS, SECALE CORNUTUM, THLASPI BURSA-PASTORIS, TRILLIUM PENDULUM.
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 9a646b7e-23dd-c2e5-e053-2995a90a66c1
SPL ID b5aae85f-4c52-e3b4-e053-2995a90adb9b
Version 2
Effective date 2020-12-04
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:34 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Mega Menses openfda.brand_name generic name APIS MELLIFICA, HAMAMELIS VIRGINIANA, HYDRASTIS CANADENSIS, ALETRIS FARINOSA, APOCYNUM CANNABINUM, CINCHONA OFFICINALIS, CINNAMOMUM, CONIUM MACULATUM, HELONIAS DIOICA, LILIUM TIGRINUM, MILLEFOLIUM, PHOSPHORUS, SECALE CORNUTUM, THLASPI BURSA-PASTORIS, TRILLIUM PENDULUM. openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-4786-1 openfda.package_ndc ndc product 55714-4786 openfda.product_ndc ndc11 package 55714478601 derived:openfda.package_ndc spl id b5aae85f-4c52-e3b4-e053-2995a90adb9b id spl set id 9a646b7e-23dd-c2e5-e053-2995a90a66c1 set_id unii 27YLU75U4W openfda.unii unii 2FXJ6SW4PK openfda.unii unii 5S29HWU6QB openfda.unii unii AHW6F0T2X0 openfda.unii unii Q28R5GF371 openfda.unii unii W0X9457M59 openfda.unii unii X67Z2963PI openfda.unii unii O021JGR97X openfda.unii unii ZW3Z11D0JV openfda.unii unii S003A158SB openfda.unii unii 7S82P3R43Z openfda.unii unii DQV54Y5H3U openfda.unii unii 2F92409L9Z openfda.unii unii 01G9XEA93N openfda.unii unii T7S323PKJS 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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.