FDA label 4e813d96-ba8e-b750-e063-6294a90ad591

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
2b8b2581-0be9-422c-b6f7-8f988e109378
SPL ID
4e813d96-ba8e-b750-e063-6294a90ad591
Version
2
Effective date
2026-04-02
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 06:18:58

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, damaged, or irritated skin ● with a heating pad ● if you are allergic to capsicum or chili peppers ● if allergic to bee stings When using this product ● avoid contact with the eyes or mucous membranes ● do not bandage tightly ● a transient burning sensation may occur upon application but generally disappears in several days ● do not expose the treated area to heat or direct sunlight Stop use and ask a doctor if ● condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days ● redness is present or irritation develops ● a severe burning sensation occurs 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.