FDA label 1cd4feb4-bf3c-f55e-e063-6294a90a2642

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
6282442b-353e-bf51-e053-2a91aa0a266a
SPL ID
1cd4feb4-bf3c-f55e-e063-6294a90a2642
Version
10
Effective date
2024-07-09
Source export date
2026-11-06
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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:02:34

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 • if allergic to iodine • in the eyes • on children less than 3 years old Ask a doctor before use if injuries are • deep or puncture wounds • serious burns Stop use and ask a doctor if • redness, irritation, swelling or pain persists or increases • infection occurs Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately. Avoid excessive heat. Store at room temperature.

Reported adverse events (FAERS/openFDA)#

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