FDA label 0a12e650-6dc6-41f5-8f24-7d8bb8c63db6

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
edd8c8ad-914b-4e18-812c-9f6864115c72
SPL ID
0a12e650-6dc6-41f5-8f24-7d8bb8c63db6
Version
2
Effective date
2017-01-26
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:51:49

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 As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product. Severe or persistent sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult a physician promptly. Do not use more than 2 days or administer to children under 12 years of age unless directed by a physician. The use of this dispenser by more than one person may spread infection. Keep this and all medication out of the reach of children. Allergic skin reaction can occur in vary rare cases, in which case use of the product should be discontinued. Do not use in known sensitivity to any of the ingredients of Vinceel.

Reported adverse events (FAERS/openFDA)#

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