FDA.reportPublic FDA data

MediChoice 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
MediChoice Povidone-Iodine
Generic name
POVIDONE-IODINE
Manufacturer
O&M HALYARD, INC.
Product type
HUMAN OTC DRUG
SPL set ID
959332db-d522-450b-b09e-be6a998899db
SPL ID
40b408a2-c8b4-36db-e063-6394a90ae959
Version
5
Effective date
2025-10-09
Source export date
2026-08-01
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/2026-08-01/5a565ce64c898c83223b815b9579cd46fb0c6d54977c3cace2133e40124f7fbb/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:10:32
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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 Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately. Ask a doctor before use if injuries are deep wounds, puncture wounds, or serious burns. Stop use and ask a doctor if infection occurs or if redness, irritation, swelling or pain persists or increases.