FDA label 2e1080c7-62cf-4813-9a90-ca9c039df97e

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
389264a4-1353-4282-adcf-17b06f361409
SPL ID
2e1080c7-62cf-4813-9a90-ca9c039df97e
Version
9
Effective date
2020-01-02
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:33:45

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

<paragraph>Do not use if allergic to iodine For external use only Ask a doctor before use if injuries are deep or punture wounds serious burns Stop use and ask a doctor if redness, irritation, swelling or pain persists or increases infection occurs Do not use in eyes Avoid pooling beneath patient Keep out of reach of children In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.<paragraph>

Reported adverse events (FAERS/openFDA)#

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