Povidone Iodine Prep Pad

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 Prep Pad
Generic name
POVIDONE-IODINE
Manufacturer
Jianerkang Medical Co., Ltd
Product type
HUMAN OTC DRUG
SPL set ID
47a504b8-b0c0-030a-e054-00144ff88e88
SPL ID
085bd3da-9cdd-fe96-e063-6294a90ab572
Version
5
Effective date
2023-10-23
Source export date
2026-10-27
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:12:21
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 apply over large areas of the body. use on individuals who are allergic or sensitive to iodine. Stop use and consult a doctor if the condition persists or gets worse for use longer than 1 week. Ask a doctor in case of deep or puncture wounds, animal bites,serious burns. Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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