FDA label 2b35c722-769f-89b1-e063-6294a90ad717

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)

SPL set ID: 6ee3fcda-15e5-3754-8ea9-39ba03359ad7
SPL ID: 2b35c722-769f-89b1-e063-6294a90ad717
Version: 5
Effective date: 2025-01-08
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:58

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		2b35c722-769f-89b1-e063-6294a90ad717	id
spl set id		6ee3fcda-15e5-3754-8ea9-39ba03359ad7	set_id

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 Do not use this product for more than 7 days unless directed by a dentist or doctor in children under 12 years of age unless directed by a dentist or doctor if you are allergic to povidone-iodine or any other ingredients in this product if you have any thyroid conditions When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water. If irritation persists, consult a doctor do not swallow do not use with hydrogen peroxide Stop use and ask a doctor or dentist if symptoms do not improve in 7 days irritation, pain, or redness persists or worsens swelling, rash, or fever develops

Reported adverse events (FAERS/openFDA)#

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