Home FDA labels b7adba46-235d-4d94-9184-fe03eaf54102 T-Relief Extra Strength 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 Extra Strength
Generic name CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP, COMFREY ROOT, ACONITUM NAPELLUS, ECHINACEA, UNSPECIFIED, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, ARNICA MONTANA, BELLIS PERENNIS AND HYPERICUM PERFORATUM
Manufacturer MediNatura Inc
Product type HUMAN OTC DRUG
SPL set ID 01804104-32c2-4011-a2e4-0f4e74bd974d
SPL ID b7adba46-235d-4d94-9184-fe03eaf54102
Version 4
Effective date 2023-09-28
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:14 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 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name T-Relief Extra Strength openfda.brand_name generic name CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP, COMFREY ROOT, ACONITUM NAPELLUS, ECHINACEA, UNSPECIFIED, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, ARNICA MONTANA, BELLIS PERENNIS AND HYPERICUM PERFORATUM openfda.generic_name manufacturer name MediNatura Inc openfda.manufacturer_name ndc package 62795-2010-4 openfda.package_ndc ndc product 62795-2010 openfda.product_ndc ndc11 package 62795201004 derived:openfda.package_ndc spl id b7adba46-235d-4d94-9184-fe03eaf54102 id spl set id 01804104-32c2-4011-a2e4-0f4e74bd974d 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 If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted . Do not use if known sensitivity to T-Relief TM or any of its ingredients exists.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.