FDA label 08aaff6a-1d51-41a6-bec2-072826cf5085

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
421ff22c-6521-463b-b324-173cc234e1f7
SPL ID
08aaff6a-1d51-41a6-bec2-072826cf5085
Version
1
Effective date
2015-05-05
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:02:03

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

Warning - For external use only. In case of accidental ingestion, get help or contact a poison control center immediately. Do not use on irritated skin in or near eyes or mucous membranes on wounds or damaged skin if prone to allergic reaction from any ingredient on large area of the body Ask a doctor or pharmacist before use if you are taking any other medication or drinking alcohol. Stop use and ask a doctor if condition worsens or clears up and occurs again, if symptoms persist for more than 7 days or irritation or severe burning occurs. If pregnant or breast-feeding ask a health professional before use. Keep at room temperature.

Reported adverse events (FAERS/openFDA)#

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