Home FDA labels d44bff7e-57cc-a6fa-e053-2a95a90a4e04 Traulevium 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 Traulevium
Generic name BELLADONNA, ARNICA MONTANA RADIX, ACONITUM NAPELLUS, CHAMOMILLA, SYMPHYTUM OFFICINALE, CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, MILLEFOLIUM, HEPAR SULPHURIS CALCAREUM, MERCURIUS SOLUBILIS, HYPERICUM PERFORATUM, BELLIS PERENNIS, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA.
Manufacturer Medical Technology Products, Inc.
Product type HUMAN OTC DRUG
SPL set ID 6123d145-4edf-4ecd-8b30-196e52273127
SPL ID d44bff7e-57cc-a6fa-e053-2a95a90a4e04
Version 4
Effective date 2021-12-29
Source export date 2026-10-27
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/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:15:30 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 Traulevium openfda.brand_name generic name BELLADONNA, ARNICA MONTANA RADIX, ACONITUM NAPELLUS, CHAMOMILLA, SYMPHYTUM OFFICINALE, CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, MILLEFOLIUM, HEPAR SULPHURIS CALCAREUM, MERCURIUS SOLUBILIS, HYPERICUM PERFORATUM, BELLIS PERENNIS, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA. openfda.generic_name manufacturer name Medical Technology Products, Inc. openfda.manufacturer_name ndc package 70857-002-10 openfda.package_ndc ndc product 70857-002 openfda.product_ndc ndc11 package 70857000210 derived:openfda.package_ndc spl id d44bff7e-57cc-a6fa-e053-2a95a90a4e04 id spl set id 6123d145-4edf-4ecd-8b30-196e52273127 set_id unii 2FXJ6SW4PK openfda.unii unii XK4IUX8MNB openfda.unii unii 324Y4038G2 openfda.unii unii O80TY208ZW openfda.unii unii 18E7415PXQ openfda.unii unii 2HU33I03UY openfda.unii unii M9VVZ08EKQ openfda.unii unii VB06AV5US8 openfda.unii unii WQZ3G9PF0H openfda.unii unii QI7G114Y98 openfda.unii unii U0NQ8555JD openfda.unii unii G0R4UBI2ZZ openfda.unii unii T7S323PKJS openfda.unii unii 1MBW07J51Q 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 symptoms worsen or persist for more than a week, a healthcare provider should be consulted. Do not use if known sensitivity to Traulevium or any of its ingredients exists. Keep out of the reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding , ask a healthcare provider before use. Keep out of reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.