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 PREP PAD
Manufacturer
Hua Jing Medical Supplies INC.
Product type
HUMAN OTC DRUG
SPL set ID
4a65fe55-e870-2576-e063-6294a90ae929
SPL ID
4a65bffe-71ec-8684-e063-6394a90a7327
Version
1
Effective date
2026-02-10
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:19:01
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 Warnings and Precautions: This product is for external use only. (Avoid use on mucous membranes such as eyes and lips. If redness, swelling, heat, pain, or other discomfort occurs, discontinue use immediately.)

Reported adverse events (FAERS/openFDA)#

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