IODDO IODINE

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)

Brand name
IODDO IODINE
Generic name
IODINE
Manufacturer
EVI LABS
Product type
HUMAN OTC DRUG
SPL set ID
4af8552c-1f2b-84ad-e063-6394a90abb62
SPL ID
4af8552c-1f2c-84ad-e063-6394a90abb62
Version
1
Effective date
2026-02-16
Source export date
2026-10-30
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:01:28
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 4 matching rows.

warnings

Warnings For external use only. Flammable: Keep away from sparks, heat, or flame

warnings

Ask a doctor before use If you have deep or puncture wounds, animal bites, or serious burns.

warnings

When using this product Do not use in the eyes or apply over large areas of the body. Do not use longer than 1 week unless directed by a doctor.

warnings

Stop use and ask a doctor If the conditions persist or get worse.

Reported adverse events (FAERS/openFDA)#

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