FDA label 0e3cb332-0192-23b2-e063-6294a90aed38

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)

SPL set ID
ca91bdca-0004-6617-e053-2a95a90ad7a0
SPL ID
0e3cb332-0192-23b2-e063-6294a90aed38
Version
3
Effective date
2024-01-05
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:34:48

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 use on wounds or damaged skin if you are allergic to any ingredients of this product with a heating pad with, or at the same time as, other external analgesic products Ask a doctor before use if you are allergic to any ingredients in this product. When using this product do not use other than directed avoid contact with eyes, mucous membranes, and rashes Stop use and ask a doctor if rash, itching, or excessive skin irritation develops condition worsens symptoms persist for longer than 7 days symptoms clear up and reoccur within a few days If pregnant or breast-feeding, ask a health professional before use. Caution: This product contains natural rubber latex which may cause allergic reactions.

Reported adverse events (FAERS/openFDA)#

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