FDA.reportPublic FDA data

FDA label fde0012f-0f00-4d01-b3fc-2eabb4061dea

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
4b743662-1ac0-4682-86d0-5488e72f3095
SPL ID
fde0012f-0f00-4d01-b3fc-2eabb4061dea
Version
1
Effective date
2011-11-15
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 05:51:45

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

• Do not use in or near the eyes • Do use in large amount particularly over the raw surfaces or blisters Stop use and Ask Doctors if • Allergic reactions occurs • Condition worsen and does not improve • Symptoms clean up and returns within few day • itching, redness, burning , swelling or other symptoms occurs • Keep both used and unused medicine out of the reach of children or pets • If swallowed get medical attention right away Call your doctor immediately.

Reported adverse events (FAERS/openFDA)#

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