FDA label 4b610b6c-76d2-48e8-b123-0e8e064fefd7

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
f00a28d4-8702-44bd-986f-a446de5949f0
SPL ID
4b610b6c-76d2-48e8-b123-0e8e064fefd7
Version
2
Effective date
2015-02-23
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:16

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 Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomitting may be serious. Consult a healthcare provider promptly. Do not use more than 2 days. This product contains ethanol and should not be inhaled. In rare cases allergic reactions may occur. If pregnant or breast-feeding , ask a healthcare provider before use. Keep out of reach of children . The use of this dispenser by more than one person may spread infection. If symptoms persist or worsen, a healthcare provider should be consulted. Do not use if known sensitivity to Reboost or any of its ingredients exists.

Reported adverse events (FAERS/openFDA)#

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