FDA label 020d568a-3288-4972-9cac-6cb4107efa21

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
bddbc4bd-61eb-4a00-8f3e-16bbc469f9cb
SPL ID
020d568a-3288-4972-9cac-6cb4107efa21
Version
1
Effective date
2020-09-23
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:19

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 When using this product • Avoid getting into the eyes. • In case of eye contact immediately flush eyes thoroughly with water. Stop use and ask a doctor if • Irritation or redness develops • Condition persist for more than 72 hours • Redness is present Keep out of reach of children. In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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