Home FDA labels 3a35f76b-50a4-4268-9147-b4c459d35379 Vascular 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 Vascular HP
Generic name AESCULUS HIPPOCASTANUM, COLLINSONIA CANADENSIS, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, PULSATILLA (PRATENSIS), ARNICA MONTANA, CARBO VEGETABILIS, GRAPHITES, HYDROFLUORICUM ACIDUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PAEONIA OFFICINALIS, SEPIA
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 0519549f-4591-46ae-ae55-6b395ae63a6d
SPL ID 3a35f76b-50a4-4268-9147-b4c459d35379
Version 4
Effective date 2024-10-31
Source export date 2026-10-12
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:44:47 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 Vascular HP openfda.brand_name generic name AESCULUS HIPPOCASTANUM, COLLINSONIA CANADENSIS, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, PULSATILLA (PRATENSIS), ARNICA MONTANA, CARBO VEGETABILIS, GRAPHITES, HYDROFLUORICUM ACIDUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PAEONIA OFFICINALIS, SEPIA openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0508-1 openfda.package_ndc ndc product 44911-0508 openfda.product_ndc ndc11 package 44911050801 derived:openfda.package_ndc spl id 3a35f76b-50a4-4268-9147-b4c459d35379 id spl set id 0519549f-4591-46ae-ae55-6b395ae63a6d set_id unii 2P3VWU3H10 openfda.unii unii 269XH13919 openfda.unii unii O80TY208ZW openfda.unii unii 8R564U2E1P openfda.unii unii 4QQN74LH4O openfda.unii unii 411VRN1TV4 openfda.unii unii QDL83WN8C2 openfda.unii unii O2630F3XDR openfda.unii unii 3C18L6RJAZ openfda.unii unii RGL5YE86CZ openfda.unii unii VB06AV5US8 openfda.unii unii 8E272251DI 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: 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.