FDA label a51f78fc-c6dc-43bd-b963-5e62533acbe7

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
a6e4abda-00d3-4219-be0e-f914610f6fe9
SPL ID
a51f78fc-c6dc-43bd-b963-5e62533acbe7
Version
1
Effective date
2011-01-14
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:04:40

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. WHEN USING THIS PRODUCT CONTACT WITH EYES SHOULD BE AVOIDED AND SHOULD THIS OCCUR, THE EYES SHOULD BE FLUSHED WITH WATER. IF IRRITATION DEVELOPS OR INCREASES, USE OF THE PRODUCT SHOULD BE DISCONTINUED. IF IRRITATION PERSISTS FOR MORE THAN 5 DAYS, CONSULT A DOCTOR. IF SWALLOWED, GET 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.