Medline

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
Medline
Generic name
POVIDONE-IODINE
Manufacturer
Medline Industries, LP
Product type
HUMAN OTC DRUG
SPL set ID
11fd1661-1b8c-b65b-e063-6394a90af89b
SPL ID
1cea06a9-c416-d705-e063-6394a90a87ef
Version
2
Effective date
2024-07-01
Source export date
2026-10-27
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:56:47
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 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 Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately. Avoid excessive heat. Protect from freezing, avoid excessive heat. Temperature limits: 15˚C-30˚C. Stop use and ask a doctor if redness, irritation, swelling or pain persists or increases infection occurs

Reported adverse events (FAERS/openFDA)#

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