Iodine Prep Pad Antiseptic

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
Iodine Prep Pad Antiseptic
Generic name
POVIDONE-IODINE
Manufacturer
Yiwu Ori-Power Medtech Co.,Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
0fdded64-4e89-d28c-e063-6394a90a7b8f
SPL ID
48d5a48f-36f5-6ebd-e063-6394a90ab435
Version
3
Effective date
2026-01-01
Source export date
2026-10-30
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/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:08:52
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If pain, irritation, redness, swelling, or infection develops, discontinue use and consult physician. Keep Out Of Reach Of Children In case of accidental swallowing, seek medical help and contact poison control immediately.

Reported adverse events (FAERS/openFDA)#

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