FDA label ba20a596-6dd2-42a1-9faf-d012f7f59c32

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
548452d1-1c35-468e-a424-b14b6e7cbf33
SPL ID
ba20a596-6dd2-42a1-9faf-d012f7f59c32
Version
1
Effective date
2020-05-14
Source export date
2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:44

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

Warning For external use only Do not use ▪ in the eyes. ▪ if you are allergic to any of the ingredients. When using this product if eye contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours. Keep out of reach of children. ▪ If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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