Povidone-Iodine Scrub Solution

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 Scrub Solution
Generic name
POVIDONE-IODINE
Manufacturer
Changzhou Maokang Medical Products Co., Ltd
Product type
HUMAN OTC DRUG
SPL set ID
efa7f9f6-ae02-4104-bb9e-16e1ffd2be7a
SPL ID
5473c5d1-7396-d2a3-e063-6294a90a2788
Version
4
Effective date
2026-06-17
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:17:12
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 Do not use if allergic to iodine do not use in the eye Stop use and ask a doctor if redness,irritation,swelling or pain persist or increases infection occurs Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a Poison Control Center immediately. Avoid pooling beneath patient.

Reported adverse events (FAERS/openFDA)#

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