Home FDA labels 295923b1-79ff-c09c-e063-6294a90abedc Tommie Copper Pain Relief Roller 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 Tommie Copper Pain Relief Roller
Generic name CAMPHOR 3.5%, MENTHOL 3.5%
Manufacturer Tommie Copper, Inc.
Product type HUMAN OTC DRUG
SPL set ID b4cd4fed-e8c8-db85-e053-2995a90a708b
SPL ID 295923b1-79ff-c09c-e063-6294a90abedc
Version 3
Effective date 2024-12-15
Source export date 2026-10-27
Source partition 5
Source file https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:00:08 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 · 14 matching rows.
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Warnings sections page 1 of 1 · 1 matching rows.
warnings For external use only. Flammable-- Do not use while smoking or near heat or flame. When using this product avoid contact with eyes, do not apply to wounds or damaged skin, and do not bandage tightly. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.