OP First Aid Series 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
OP First Aid Series Povidone Iodine Prep Pad
Generic name
POVIDONE-IODINE
Manufacturer
Yiwu Ori-Power Medtech Co.,Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
b43ae55f-dc21-09b2-e053-2995a90adf4c
SPL ID
48dacfc0-8e00-4fe1-e063-6394a90aa29d
Version
4
Effective date
2026-01-01
Source export date
2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:48
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 Avoid contact with eyes.If happens,rinse thoroughly with water. Stop use In case of deep or puncture wounds or serious burns,and if pain,irritation, redness, swelling,or infection occurs,discontinue use and contact a physician. 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.