FDA label 2b22e023-7e56-72c0-e063-6294a90a8104

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
dfc88cae-cf19-4a9e-a707-160938979b3c
SPL ID
2b22e023-7e56-72c0-e063-6294a90a8104
Version
2
Effective date
2025-01-07
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:57:37

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: Use only as directed. For external use only If condition worsens, or if symptoms persist for more than 7 days or clears up and occur again within a few days, discontinue use of this product and consult a physician. Avoid contact with eyes or mucous membranes Pregnancy - Breast feeding warning: If pregnant or breast feeding, ask a physician before use Do not use with other topical products Do not use on open wounds Keep away from excessive heat or open flame KEEP AWAY FROM CHILDREN If swallowed, seek professional help and contact Poison Control immediately.

Reported adverse events (FAERS/openFDA)#

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