Saninta 10% Povidone-Iodine

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
Saninta 10% Povidone-Iodine
Generic name
POVIDONE-IODINE SOLUTION
Manufacturer
LL Pharma
Product type
HUMAN OTC DRUG
SPL set ID
bd344007-895e-30d6-e053-2a95a90a019d
SPL ID
47446355-315f-6485-e063-6294a90a0377
Version
6
Effective date
2025-12-31
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:28:26
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 use Do not use if allergic to iodine in the eyes Stop use and ask a doctor Stop use and ask a doctor if injuries are deep puncture wounds or serious burns redness, irritation, swelling or pain persists or increases infection occurs Avoid pooling beneath patient Avoid pooling beneath patient Keep out of reach of children Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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