FDA label 39ef369b-8e81-442a-9e31-55ee8b2585bf

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
757aed4e-43b9-4361-83bb-3fc4a6688d31
SPL ID
39ef369b-8e81-442a-9e31-55ee8b2585bf
Version
2
Effective date
2012-01-04
Source export date
2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:07:18

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 Flammable, keep away from fire or flame. For external use only. Do not use if you are allergic to or have a known or suspected hypersensitivity to any ingredient in this product. on or near the eyes, mucous membranes, genital skin, or mouth. If product gets into the eyes, flush immediately with water. Avoid contact with broken skin. Stop use and ask doctor if irritation and redness develop. If condition persists for more than 72 hours consult a physician. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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