Profoot Pain Relief Patches

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
Profoot Pain Relief Patches
Generic name
CAMPHOR, MENTHOL, METHYL SALICYLATE
Manufacturer
Profoot, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
06f82bde-41a1-35f6-e063-6394a90a6437
SPL ID
252a0dfe-c0dc-640c-e063-6394a90a999b
Version
3
Effective date
2024-10-23
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 06:15:36

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 Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. Do not use • on wounds or damaged skin • with a heating pad • if you are allergic to any of the ingredients of this product When using this product • use only as directed • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly Stop use and ask a doctor if • rash, itching or excessive skin irritation develops • condition worsens •symptoms persist for more than 7 days • symptoms clear up and occur again within a few days If pregnant or breastfeeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.