Home FDA labels d2d95f05-1490-4ae6-9a9e-7f75a289cdf1 T-Relief 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 T-Relief
Generic name ACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP AND COMFREY ROOT
Manufacturer MediNatura Inc
Product type HUMAN OTC DRUG
SPL set ID edb2fe62-e990-4cef-8600-9d1b85bffa5a
SPL ID d2d95f05-1490-4ae6-9a9e-7f75a289cdf1
Version 6
Effective date 2023-09-27
Source export date 2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:28:14 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name T-Relief openfda.brand_name generic name ACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP AND COMFREY ROOT openfda.generic_name manufacturer name MediNatura Inc openfda.manufacturer_name ndc package 62795-7005-5 openfda.package_ndc ndc package 62795-7005-6 openfda.package_ndc ndc product 62795-7005 openfda.product_ndc ndc11 package 62795700505 derived:openfda.package_ndc ndc11 package 62795700506 derived:openfda.package_ndc spl id d2d95f05-1490-4ae6-9a9e-7f75a289cdf1 id spl set id edb2fe62-e990-4cef-8600-9d1b85bffa5a set_id unii 2FXJ6SW4PK openfda.unii unii XK4IUX8MNB openfda.unii unii O80TY208ZW openfda.unii unii 18E7415PXQ openfda.unii unii 2HU33I03UY openfda.unii unii N94C2U587S openfda.unii unii M9VVZ08EKQ openfda.unii unii 4N9P6CC1DX openfda.unii unii WQZ3G9PF0H openfda.unii unii U0NQ8555JD openfda.unii unii 5EF0HWI5WU openfda.unii unii G0R4UBI2ZZ openfda.unii unii T7S323PKJS 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 For external use only. Do not apply over open wounds or broken skin. If symptoms persist or worsen, or if a rash develops, a health professional should be consulted. In rare cases, allergic skin reactions may develop. Do not use if known sensitivity to T-Relief TM 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.