Home FDA labels 52ba408a-5552-4842-9070-22e268055e29 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 ACONITUM NAPELLUS, ARNICA MONTANA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA, UNSPECIFIED, ECHINACEA PURPUREA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, CALCIUM SULFIDE, HYPERICUM PERFORATUM, MERCURIUS SOLUBILIS, ACHILLEA MILLEFOLIUM AND COMFREY ROOT
Manufacturer Biologische Heilmittel Heel
Product type HUMAN OTC DRUG
SPL set ID 9ff5c743-0e8f-4416-9964-c92b3abb54dd
SPL ID 52ba408a-5552-4842-9070-22e268055e29
Version 3
Effective date 2023-03-06
Source export date 2026-10-12
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 03:12:51 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 Traumeel openfda.brand_name generic name ACONITUM NAPELLUS, ARNICA MONTANA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA, UNSPECIFIED, ECHINACEA PURPUREA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, CALCIUM SULFIDE, HYPERICUM PERFORATUM, MERCURIUS SOLUBILIS, ACHILLEA MILLEFOLIUM AND COMFREY ROOT openfda.generic_name manufacturer name Biologische Heilmittel Heel openfda.manufacturer_name ndc package 51885-9487-8 openfda.package_ndc ndc product 51885-9487 openfda.product_ndc ndc11 package 51885948708 derived:openfda.package_ndc spl id 52ba408a-5552-4842-9070-22e268055e29 id spl set id 9ff5c743-0e8f-4416-9964-c92b3abb54dd 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 WQZ3G9PF0H openfda.unii unii QI7G114Y98 openfda.unii unii U0NQ8555JD openfda.unii unii G0R4UBI2ZZ openfda.unii unii T7S323PKJS 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 Warning Warnings: For external use only. Cetylstearyl alcohol may cause local skin reactions, i.e. contact dermatitis. Do not apply over large areas of the body. Do not apply over open wounds or broken skin. If symptoms persist or worsen, or if a rash develops, a physician should be consulted. Do not use if known sensitivity to Traumeel® ointment 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, ask a health professional before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.