Home FDA labels f4878551-dc72-456e-b285-028b5bfdafcb Gynestat 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 Gynestat
Generic name CIMICIFUGA RACEMOSA, EUCALYPTUS GLOBULUS, ARGENTUM NITRICUM, AURUM MURIATICUM NATRONATUM, BORAX, CALCAREA CARBONICA, KALI BICHROMICUM, KREOSOTUM, LILIUM TIGRINUM, MERCURIUS SOLUBILIS, PULSATILLA (PRATENSIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 3af1d2f1-b3f3-4135-9148-726d08bbd5d4
SPL ID f4878551-dc72-456e-b285-028b5bfdafcb
Version 1
Effective date 2024-08-02
Source export date 2026-10-12
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:59:48 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 Gynestat openfda.brand_name generic name CIMICIFUGA RACEMOSA, EUCALYPTUS GLOBULUS, ARGENTUM NITRICUM, AURUM MURIATICUM NATRONATUM, BORAX, CALCAREA CARBONICA, KALI BICHROMICUM, KREOSOTUM, LILIUM TIGRINUM, MERCURIUS SOLUBILIS, PULSATILLA (PRATENSIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0716-1 openfda.package_ndc ndc product 44911-0716 openfda.product_ndc ndc11 package 44911071601 derived:openfda.package_ndc spl id f4878551-dc72-456e-b285-028b5bfdafcb id spl set id 3af1d2f1-b3f3-4135-9148-726d08bbd5d4 set_id unii 00543AP1JV openfda.unii unii 324Y4038G2 openfda.unii unii 91MBZ8H3QO openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii 95IT3W8JZE openfda.unii unii 2E32821G6I openfda.unii unii X67Z2963PI openfda.unii unii 8E272251DI openfda.unii unii T4423S18FM openfda.unii unii 3JYG22FD73 openfda.unii unii 7FT6QUT299 openfda.unii unii K73E24S6X9 openfda.unii unii S546YLW6E6 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: Stop use and ask a doctor if symptoms persist for more than 7 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING Store in a cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.