FDA.reportPublic FDA data

FDA label f42ad3c6-61cf-93da-e053-2a95a90a9fdc

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
ab3eea55-4e13-4f60-9db2-0380beb0f18c
SPL ID
f42ad3c6-61cf-93da-e053-2a95a90a9fdc
Version
2
Effective date
2023-02-08
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:52

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 For external use only Do not use this product in the eyes When using this product • Prolonged exposure to wet solution may cause irritation or, rarely, severe skin reactions • In pre-operative prepping avoid “pooling” beneath the patient Stop use and ask a doctor • If irritation and redness develop • In rare instances of local irritation or sensitivity 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.