Home FDA labels f88d94e1-d8ab-4268-8935-9cc92c666154 Trauma Remedy 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 Trauma Remedy
Generic name CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, HYPERICUM PERFORATUM, MILLEFOLIUM, CALENDULA OFFICINALIS, ARNICA MONTANA, BELLIS PERENNIS, RHUS TOX, BRYONIA (ALBA), CLEMATIS VITALBA, FOLIA, HEPAR SULPHURIS CALCAREUM, ORNITHOGALUM UMBELLATUM, PRUNUS CERASIFERA, FLOS, CARBO VEGETABILIS
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID d8610c75-2d98-4810-8265-96f8f151b61f
SPL ID f88d94e1-d8ab-4268-8935-9cc92c666154
Version 4
Effective date 2024-03-07
Source export date 2026-10-12
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:32:57 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Trauma Remedy openfda.brand_name generic name CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, HYPERICUM PERFORATUM, MILLEFOLIUM, CALENDULA OFFICINALIS, ARNICA MONTANA, BELLIS PERENNIS, RHUS TOX, BRYONIA (ALBA), CLEMATIS VITALBA, FOLIA, HEPAR SULPHURIS CALCAREUM, ORNITHOGALUM UMBELLATUM, PRUNUS CERASIFERA, FLOS, CARBO VEGETABILIS openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1536-1 openfda.package_ndc ndc product 43742-1536 openfda.product_ndc ndc11 package 43742153601 derived:openfda.package_ndc spl id f88d94e1-d8ab-4268-8935-9cc92c666154 id spl set id d8610c75-2d98-4810-8265-96f8f151b61f set_id unii 2P3VWU3H10 openfda.unii unii 2FXJ6SW4PK openfda.unii unii 0KD7R09EAS openfda.unii unii XK4IUX8MNB openfda.unii unii O80TY208ZW openfda.unii unii 18E7415PXQ openfda.unii unii 490F0009OP openfda.unii unii 2HU33I03UY openfda.unii unii 9NS3M2Y78S openfda.unii unii 6IO182RP7A openfda.unii unii VB06AV5US8 openfda.unii unii T7J046YI2B 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 pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.