Lidozen

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
Lidozen
Generic name
LIDOCAINE HYDROCHLORIDE, MENTHOL
Manufacturer
Proficient Rx LP
Product type
HUMAN OTC DRUG
SPL set ID
1ebb45e5-4541-4c95-abe1-661ef763a610
SPL ID
de5d688d-8c71-4bf5-999c-17a3f323f854
Version
8
Effective date
2023-11-01
Source export date
2026-11-06
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:31:29
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. • Avoid contact with eyes. • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. • Do not use in large quantities, particularly over raw surfaces or blistered areas. • ​If pregnant or breast-feeding, ​ ask a health professional before use. Keep out of reach of children. • If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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