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
Medline Industries, LP
Product type
HUMAN OTC DRUG
SPL set ID
2b95078e-2caf-7005-e054-00144ff88e88
SPL ID
41c65656-ff98-67e5-e063-6394a90a6079
Version
8
Effective date
2025-10-22
Source export date
2026-10-27
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:41:27
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 if you are allergic to iodine or any of the other ingredients in the product When using this product prolonged exposure to wet solution may cause irritation or, rarely, severe skin reactions in pre-operative prepping, avoid “pooling” beneath the patient Stop use and ask a doctor if irritation and redness develop if condition persists for more than 72 hours 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.