Home FDA labels 40d598a1-692c-4e35-86d8-5faea2327c3c Varico HP 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 Varico HP
Generic name AESCULUS HIPPOCASTANUM, CALCAREA FLUORICA, CARBO VEGETABILIS, CARDUUS MARIANUS, HAMAMELIS VIRGINIANA, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, PAEONIA OFFICINALIS, PULSATILLA (PRATENSIS), SECALE CORNUTUM, SEPIA, STAPHYSAGRIA, ZINCUM METALLICUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 83aff417-88f3-4c03-b5fc-9c0df265d3c3
SPL ID 40d598a1-692c-4e35-86d8-5faea2327c3c
Version 2
Effective date 2024-05-08
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 05:37:08 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 Varico HP openfda.brand_name generic name AESCULUS HIPPOCASTANUM, CALCAREA FLUORICA, CARBO VEGETABILIS, CARDUUS MARIANUS, HAMAMELIS VIRGINIANA, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, PAEONIA OFFICINALIS, PULSATILLA (PRATENSIS), SECALE CORNUTUM, SEPIA, STAPHYSAGRIA, ZINCUM METALLICUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0667-1 openfda.package_ndc ndc product 44911-0667 openfda.product_ndc ndc11 package 44911066701 derived:openfda.package_ndc spl id 40d598a1-692c-4e35-86d8-5faea2327c3c id spl set id 83aff417-88f3-4c03-b5fc-9c0df265d3c3 set_id unii 2P3VWU3H10 openfda.unii unii O3B55K4YKI openfda.unii unii 00543AP1JV openfda.unii unii 8R564U2E1P openfda.unii unii QDL83WN8C2 openfda.unii unii 3C18L6RJAZ openfda.unii unii U946SH95EE openfda.unii unii 8E272251DI openfda.unii unii VSW71SS07I openfda.unii unii J41CSQ7QDS openfda.unii unii 01G9XEA93N openfda.unii unii C88X29Y479 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: 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.