Home FDA labels 52582be9-3f44-4423-e063-6294a90ae8cc Traumeel 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 Traumeel
Generic name ATROPA BELLADONNA,ECHINACEA, UNSPECIFIED,ARNICA MONTANA ROOT,ACONITUM NAPELLUS,BELLIS PERENNIS,CALENDULA OFFICINALIS FLOWERING TOP,CALCIUM SULFIDE,HYPERICUM PERFORATUM,COMFREY ROOT,MATRICARIA RECUTITA,HAMAMELIS VIRGINIANA LEAF,ECHINACEA PURPUREA,MERCURIUS SOLUBILIS,ACHILLEA MILLEFOLIUM
Manufacturer MediNatura Inc
Product type HUMAN OTC DRUG
SPL set ID 39630b57-28b1-486b-a4ff-4af65324454f
SPL ID 52582be9-3f44-4423-e063-6294a90ae8cc
Version 5
Effective date 2026-05-21
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 05:15:20 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 Traumeel openfda.brand_name generic name ATROPA BELLADONNA,ECHINACEA, UNSPECIFIED,ARNICA MONTANA ROOT,ACONITUM NAPELLUS,BELLIS PERENNIS,CALENDULA OFFICINALIS FLOWERING TOP,CALCIUM SULFIDE,HYPERICUM PERFORATUM,COMFREY ROOT,MATRICARIA RECUTITA,HAMAMELIS VIRGINIANA LEAF,ECHINACEA PURPUREA,MERCURIUS SOLUBILIS,ACHILLEA MILLEFOLIUM openfda.generic_name manufacturer name MediNatura Inc openfda.manufacturer_name ndc package 62795-9488-2 openfda.package_ndc ndc product 62795-9488 openfda.product_ndc ndc11 package 62795948802 derived:openfda.package_ndc spl id 52582be9-3f44-4423-e063-6294a90ae8cc id spl set id 39630b57-28b1-486b-a4ff-4af65324454f set_id unii 2FXJ6SW4PK openfda.unii unii XK4IUX8MNB openfda.unii unii 324Y4038G2 openfda.unii unii 18E7415PXQ openfda.unii unii 2HU33I03UY openfda.unii unii M9VVZ08EKQ openfda.unii unii 4N9P6CC1DX openfda.unii unii T07U1161SV openfda.unii unii WQZ3G9PF0H openfda.unii unii QI7G114Y98 openfda.unii unii U0NQ8555JD openfda.unii unii G0R4UBI2ZZ openfda.unii unii 1MBW07J51Q openfda.unii unii MUE8Y11327 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. If symptoms persist or worsen, a healthcare provider should be consulted. Do not use if known sensitivity to Traumeel® or any of its ingredients exists
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.