FDA.reportPublic FDA data

FDA label f0033086-4ab3-b3e3-e053-2995a90ad171

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
41f7e33d-30a1-5d2d-e054-00144ff8d46c
SPL ID
f0033086-4ab3-b3e3-e053-2995a90ad171
Version
3
Effective date
2022-12-17
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:14:30

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 For External use only-hands. When using this produt.avoid contact with eyes.In case of eye contact ,flush eyes with water. Stop use and ask a doctor.if irritation or redness develops,or if condition persists for more than 72 hours. keep out of reach of children if swallowed,get medical help to contact a poison control center reght away keep out of reach of children unless under adult supervision .if seallowed ,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.