FDA.reportPublic FDA data

Prep Pad Sterile

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
Prep Pad Sterile
Generic name
POVIDONE-IODINE
Manufacturer
Changzhou Maokang Medical Products Co., Ltd
Product type
HUMAN OTC DRUG
SPL set ID
758abf53-ad8a-62ac-e053-2991aa0a8f0c
SPL ID
0a3e519c-ece5-d487-e063-6294a90a1f47
Version
6
Effective date
2023-11-15
Source export date
2026-08-01
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/5a565ce64c898c83223b815b9579cd46fb0c6d54977c3cace2133e40124f7fbb/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:09:53
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 For external use only. Do not apply to persions allergic to iodine. Do not use in the eyes. Ask a doctor before use if injuries are deep wounds, puncture wounds, serious burns. Keep out of reach of children If swallowed or gets in eyes, get medical help or contact a Poison Control Center right away.