FDA.reportPublic FDA data

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
ANTISEPTIC
Manufacturer
Dynarex Corporation
Product type
HUMAN OTC DRUG
SPL set ID
81b475e8-8da4-7b15-e053-2991aa0a6629
SPL ID
4ddd1f85-ed0e-bdff-e063-6394a90a4da3
Version
8
Effective date
2026-03-25
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:06:25
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 · 2 matching rows.

warnings

Warnings For External Use Only Do not use • In the eyes or over large areas of the body • Longer than one week unless directed by a doctor Ask a doctor before use if you have • Deep or puncture wounds • Animal bites • Serious burns Stop use and ask a doctor if • Condition persists or gets worse Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

warnings

Do not use • In the eyes or over large areas of the body • Longer than one week unless directed by a doctor

Reported adverse events (FAERS/openFDA)#

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