FDA.reportPublic FDA data

Povidone-Iodine Scrub 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
Povidone-Iodine Scrub Sterile
Generic name
POVIDONE-IODINE
Manufacturer
Cardinal Health 200, Inc
Product type
HUMAN OTC DRUG
SPL set ID
c1cdc3d3-e02a-42fb-9cb2-6a1b56a3c607
SPL ID
09d693d5-ec0a-5c7c-e063-6394a90a6d74
Version
4
Effective date
2023-11-10
Source export date
2026-08-08
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-08/2ef638b6b5a68e854d11a3945e1b1aa8d0e7f812a9d69af10df01eecf2e189d0/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
b39f3b00ad50d2e1b32aaf429248c6081e8799b35bce715b4fccb8cfa1ac4546
Import run
20260810T161303Z
Imported at
2026-08-10 18:08:01
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 ​For external use only. Do not apply to persons allergic to iodine Do not use • in the eyes Ask a doctor before use if injuries are • deep wounds • puncture wounds • serious burns Stop use and ask a doctor if • irritation and redness develop • condition persists for more than 72 hours • infection occurs Avoid pooling beneath the patient. Prolonged exposure to wet solution may cause skin irritation. Keep out of reach of children. If swallowed or gets in eyes, get medical help or contact a Poison Control Center right away.