Antiseptic 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
Antiseptic Povidone Iodine Prep Pad
Generic name
POVIDONE-IODINE
Manufacturer
M-star (Hubei) Health&Care Products Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
fc76c1f3-b48e-4276-890d-5b8e5a894e62
SPL ID
1507ac3e-81e3-892c-e063-6394a90ac565
Version
1
Effective date
2024-04-01
Source export date
2026-11-06
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/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:51:07
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 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.