FDA label f49b7ea3-1101-75e0-e053-2a95a90ab354

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
a2af654b-8ec6-4990-8584-742ebc597639
SPL ID
f49b7ea3-1101-75e0-e053-2a95a90ab354
Version
6
Effective date
2023-02-13
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:58:07

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 contains alcohol which is flammable until dry Single use only Do not use if you are allergic to povidone iodine or ethyl alcohol to treat wounds or burns in eyes, mucus membranes on broken skin with electrocautery procedures Stop use and ask a doctor if the insertion site becomes red irritated swollen painful infected 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.