FDA.reportPublic FDA data

SunBurnt PLUS

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)

Brand name
SunBurnt PLUS
Generic name
LIDOCAINE HYDROCHLORIDE
Manufacturer
Quest Products, LLC.
Product type
HUMAN OTC DRUG
SPL set ID
12128c75-015d-8a72-e063-6394a90ae00a
SPL ID
12128c75-015e-8a72-e063-6394a90ae00a
Version
1
Effective date
2024-02-23
Source export date
2026-08-01
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/d245bd7ce31d1d8ed63276109973402ece6c44860774da30f25b731cd7418983/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:32:23
Harmonized routes table
Harmonized routes
TOPICAL

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 For external use only Do not use in large quantities, particularly over raw surfaces or blistered areas if you have an allergy or hypersensitivity to any ingredients Ask a doctor before use if you have severe sunburn you have a rash or broken or compromised skin When using this product Avoid contact with eyes Stop use and ask a doctor condition worsens symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.