Povidone-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
Povidone-Iodine
Generic name
POVIDONE-IODINE
Manufacturer
Mazza Healthcare, LLC
Product type
HUMAN OTC DRUG
SPL set ID
3dc3303f-54b2-4aec-8568-5e0f8eb7cb14
SPL ID
9302db32-d3ac-48cd-88ba-f6ea3c02888d
Version
2
Effective date
2024-11-21
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:44:09
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 · 1 matching rows.

warnings

Warnings For external use only Do not use in the eyes on individuals who are allergic or sensitive to iodine over large areas of the body as first aid antiseptic longer than 1 week unless directed by doctor Discontinue use if irritation and redness develop. Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns. Stop use and consult a doctor if the condition persists or gets worse. 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.