Povidone Iodine Prep Swabstick

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 Swabstick
Generic name
POVIDONE IODINE
Manufacturer
PHOENIX HEALTHCARE SOLUTIONS, LLC
Product type
HUMAN OTC DRUG
SPL set ID
8a0aba34-3f96-46b6-8521-f4388fb73edf
SPL ID
41d30914-6c97-01ea-e063-6394a90a9f03
Version
10
Effective date
2025-10-23
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:45
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 in the eyes use on individuals who are allergic or sensitive to iodine apply over large areas of the body use as a first aid antiseptic longer than 1 week unless directed by a doctor. Discontinue use if irritation and redness develop. Consult a doctor in case of deep or puncture wounds animal bites serious burns Stop use and consult a doctor if the condition persists or gets worse. 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.