FDA label 6ee89110-ae7c-4814-a8f7-5cafa703741f

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: f643f019-4fdf-4bca-a5f1-7e8b4e171572
SPL ID: 6ee89110-ae7c-4814-a8f7-5cafa703741f
Version: 7
Effective date: 2014-03-25
Source export date: 2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:42:37

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		6ee89110-ae7c-4814-a8f7-5cafa703741f	id
spl set id		f643f019-4fdf-4bca-a5f1-7e8b4e171572	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 SECTION Warnings If used for sore throat: Consult a doctor promplty if sore throat is severe or persists more than 2 daysaccompanied by : rash swelling fever headache nausea vomiting Unless directed by a doctor do not administer to children under 3 years of age. If used for sore mouth: See your dentist or doctor promptly if sore mouth symptoms do not improve in 7 days. irritation, pain, or redness persists or worsens Stop use and ask a doctor if persistent or severe inflammatino occurs, which may indicate Iodine or Phenol sensitivity. Label

Reported adverse events (FAERS/openFDA)#

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