Antiseptic Povidone-lodine 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
Antiseptic Povidone-lodine Prep Pad
Generic name
POVIDONE-IODINE
Manufacturer
Hubei Changjian Medical Products Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
2cacf2e0-0192-4e0f-88a6-e3eee3af5471
SPL ID
24348a49-917d-1ee7-e063-6394a90ab1f4
Version
4
Effective date
2024-10-11
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:43
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 Keep out of reach of children Single use only Keep out of reach of children Do not use: in the eyes over large areas of the body as a first aid antiseptic for longer than one week unless directed by a physician on individuals who are sensitive or allergic to iodine if package is damaged or open Stop use and ask a doctor if irritation, redness, or symptoms develops if the condition persists or gets worse.

Reported adverse events (FAERS/openFDA)#

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