FDA.reportPublic FDA data

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
Jianerkang Medical Co., Ltd
Product type
HUMAN OTC DRUG
SPL set ID
bbe0d44d-8752-44e6-acad-f8deeebdbf17
SPL ID
085e7fe4-e6a2-9dd9-e063-6294a90a9d87
Version
4
Effective date
2023-10-23
Source export date
2026-08-01
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/2026-08-01/928e480b2a9ec5fd356ebc3e5dcca70f0f57b8a051cfbb174a4421de39bb77a2/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:26:35
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 use on individuals who are allergic or sensitive to iodine apply over large areas of the body use as a first aid antiseptic longer than 1 week unless directed by a doctor. if irritation and redness develop. Consult a doctor in case of deep or puncture wounds animal bites serious burns. Discontinue use