FDA label ec2ee0a5-72a5-766e-e053-2995a90a60ff

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: c24e71dd-abf7-68cf-e053-2995a90a8a17
SPL ID: ec2ee0a5-72a5-766e-e053-2995a90a60ff
Version: 2
Effective date: 2022-10-29
Source export date: 2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:09:43

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		ec2ee0a5-72a5-766e-e053-2995a90a60ff	id
spl set id		c24e71dd-abf7-68cf-e053-2995a90a8a17	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 Sore throat warning If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea or vomiting, consult a doctor promptly Stop use and ask a doctor or dentist if sore mouth symptoms do not improve in 7 days If pregnant or breast-feeding, ask a health professional before use Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not exceed the recommended dosage. When using this product, try to avoid swallowing spray

Reported adverse events (FAERS/openFDA)#

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