FDA.reportPublic FDA data

sunmark Povidone-Iodine Topical

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
sunmark Povidone-Iodine Topical
Generic name
POVIDONE-IODINE
Manufacturer
Strategic Sourcing Services LLC
Product type
HUMAN OTC DRUG
SPL set ID
acc349d6-2875-4814-aa6e-828fffec7f07
SPL ID
0ce5be01-e0b9-7245-e063-6294a90acccf
Version
9
Effective date
2023-12-19
Source export date
2026-08-01
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/f23e8214fa581dc87bce024b3f15739356a8bb6f9298e3d6be38c21c662a4211/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:06:36
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 in the eyes. use longer than 1 week unless directed by a doctor. use on individuals who are allergic or sensitive to iodine. apply over large areas of the body. Stop use and consult a doctor if condition persists or gets worse. irritation and redness develop and persist for more than 72 hours. Ask a doctor in case of: deep or puncture wounds animal bites serious burns. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.