Home FDA labels d44c63cf-1825-746a-e053-2a95a90adf65 Traulevium Pain Relief Gel 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 Pain Relief Gel
Generic name ARNICA MONTANA, CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, ECHINACEA, ECHINACEA PURPUREA, CHAMOMILLA, SYMPHYTUM OFFICINALE, BELLIS PERENNIS, HYPERICUM PERFORATUM, MILLEFOLIUM, ACONITUM NAPELLUS, BELLADONNA, MERCURIUS SOLUBILIS, HEPAR SULPHURIS CALCAREUM.
Manufacturer Medical Technology Products, Inc.
Product type HUMAN OTC DRUG
SPL set ID 692daf7a-11e2-4f08-bdcf-1b9ac866d213
SPL ID d44c63cf-1825-746a-e053-2a95a90adf65
Version 5
Effective date 2021-12-29
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:22 Harmonized routes table Harmonized routes TOPICAL
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 Pain Relief Gel openfda.brand_name generic name ARNICA MONTANA, CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, ECHINACEA, ECHINACEA PURPUREA, CHAMOMILLA, SYMPHYTUM OFFICINALE, BELLIS PERENNIS, HYPERICUM PERFORATUM, MILLEFOLIUM, ACONITUM NAPELLUS, BELLADONNA, MERCURIUS SOLUBILIS, HEPAR SULPHURIS CALCAREUM. openfda.generic_name manufacturer name Medical Technology Products, Inc. openfda.manufacturer_name ndc package 70857-004-16 openfda.package_ndc ndc product 70857-004 openfda.product_ndc ndc11 package 70857000416 derived:openfda.package_ndc spl id d44c63cf-1825-746a-e053-2a95a90adf65 id spl set id 692daf7a-11e2-4f08-bdcf-1b9ac866d213 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 4N9P6CC1DX 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 Warnings For external use only. Do not apply over open wounds or broken skin. If symptoms worsen or persist for more than a week, or if a rash develops, a healthcare provider should be consulted. In rare cases, allergic skin reactions may develop. Do not use if known sensitivity to Traulevium or any of its ingredients exists. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, consult a healthcare provider before use. Keep out of the reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.