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
2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:55:32
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.