FDA label d58d3e53-208f-b9c6-e053-2a95a90a3313

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
1c21cb0a-730e-4ec0-a103-f6f70602f341
SPL ID
d58d3e53-208f-b9c6-e053-2a95a90a3313
Version
3
Effective date
2022-01-14
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:58:17

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 skin with a heating pad or bandage tightly. When using this product avoid contact with eyes or mucous membranes. Stop use and ask a doctor if condition worsens or symptoms persist more than 7 days symptoms clear and occur again with a few days excessive skin irritation develops. Keep out of reach of children. If pregnant or breast-feeding, ask a health professional before use. If swallowed, get medical help or contact a poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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