FDA.reportPublic FDA data

FDA label a379dee4-9103-4cf2-8ac7-3d11fee44bcc

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
db4c2ef4-06d4-4f86-94e2-7ec9b609bc4b
SPL ID
a379dee4-9103-4cf2-8ac7-3d11fee44bcc
Version
1
Effective date
2021-03-30
Source export date
2026-11-06
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/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:55:52

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 • Be careful not to get in your eyes. • If it gets into your eyes, immediately wash it off with clean water several times. • Wear appropriate gloves during the procedure. • Do not eat. • Keep out of reach of children. • Store in a cool place away from direct sunlight. • Recommended for single use only. • For professional use only. • Follow the recommendations. • After use, if skin irritation such as rash or itching persists, stop use and consult a doctor or pharmacist

Reported adverse events (FAERS/openFDA)#

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