FDA.reportPublic FDA data

FDA label a0dc6a50-290e-452a-9928-2a0a215df7a4

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
5fd088e3-4e49-4a04-b636-31ac0c22a1b8
SPL ID
a0dc6a50-290e-452a-9928-2a0a215df7a4
Version
1
Effective date
2021-03-30
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:13:53

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.