FDA label 128b9fee-105c-d708-e063-6294a90af495

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
ea39cd13-cacf-3d69-e053-2995a90a7906
SPL ID
128b9fee-105c-d708-e063-6294a90af495
Version
2
Effective date
2024-02-29
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:52

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 Flammable: Keep away from fire or flame Do not use on wounds or damaged skin in large quantaties with a heating pad if you are allergic to any 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 doctor if skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering condition worsens symptoms persist for more than 7 days symptoms 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.