Home FDA labels 5efc2aef-833a-4b2c-a651-6a014bd450d2 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 ACHILLEA MILLEFOLIUM, HYPERICUM PERFORATUM, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ECHINACEA, UNSPECIFIED, MATRICARIA RECUTITA, ATROPA BELLADONNA,COMFREY ROOT, ACONITUM NAPELLUS, BELLIS PERENNIS,ARNICA MONTANA, AND RUTA GRAVEOLENS FLOWERING TOP
Manufacturer MediNatura Inc
Product type HUMAN OTC DRUG
SPL set ID 1fcfd0a5-b4ff-4546-e054-00144ff8d46c
SPL ID 5efc2aef-833a-4b2c-a651-6a014bd450d2
Version 8
Effective date 2023-09-27
Source export date 2026-10-27
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:24:57 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 ACHILLEA MILLEFOLIUM, HYPERICUM PERFORATUM, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ECHINACEA, UNSPECIFIED, MATRICARIA RECUTITA, ATROPA BELLADONNA,COMFREY ROOT, ACONITUM NAPELLUS, BELLIS PERENNIS,ARNICA MONTANA, AND RUTA GRAVEOLENS FLOWERING TOP openfda.generic_name manufacturer name MediNatura Inc openfda.manufacturer_name ndc package 62795-7004-7 openfda.package_ndc ndc package 62795-7004-8 openfda.package_ndc ndc product 62795-7004 openfda.product_ndc ndc11 package 62795700408 derived:openfda.package_ndc ndc11 package 62795700407 derived:openfda.package_ndc spl id 5efc2aef-833a-4b2c-a651-6a014bd450d2 id spl set id 1fcfd0a5-b4ff-4546-e054-00144ff8d46c 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 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.