FDA label 45f26500-7af5-3d61-e063-6394a90aa130

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
93f5b6ac-14c4-4d86-839b-1604063e9401
SPL ID
45f26500-7af5-3d61-e063-6394a90aa130
Version
6
Effective date
2025-12-14
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 05:15:51

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. Avoid contact with eyes Do not use On wounds or damaged skin With heating pad Do not bandage tightly Stop use and consult a doctor if condition worsens or if symptoms persist for more than 7 days. If pregnant or breast-feeding, consult a health professional before use. This product may cause an allergic reaction for some individuals. Test on a small area before use. Keep out reach of children. If product is swallowed, seek 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.