FDA label de538e86-174d-4d08-a2a5-8b4c0cd20ef3

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
053c2bbb-16d1-44b3-b4dc-7f983903844f
SPL ID
de538e86-174d-4d08-a2a5-8b4c0cd20ef3
Version
3
Effective date
2017-01-30
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 05:40:57

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 apply to wounds or damaged skin do not bandage tightly do not use with heating pad, pack, wrap, hot water bottle or any heating element When using this product do not get into eyes avoid contact with other mucous membranes Flammable Keep from heat and flame. Discontinue 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 Keep out of reach of children. if swallowed, get medical help or contact a Poison Control center right away if pregnant or nursing, seek the advice of a health professional before using

Reported adverse events (FAERS/openFDA)#

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