FDA label d54e551d-9f7e-4e48-8068-c9e642a168d6

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
f1be69b8-8cfd-428c-aa79-eeb87e3cd3e3
SPL ID
d54e551d-9f7e-4e48-8068-c9e642a168d6
Version
1
Effective date
2013-06-25
Source export date
2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:58

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

FOR EXTERNAL USE ONLY When using this product Avoid contact with eyes, lips or mucous membranes Do not apply over deep or punctured wounds, infections or lacerations. Cautions: Irritation may occur on the face. Fair skinned individuals may experience mild stinging. Burning or peeling may occur on sensitive or irritated skin areas. If irritation occurs, Discontinue use immediately and consult a physcian for appropiate therapy.

Reported adverse events (FAERS/openFDA)#

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