ALCEMISTE

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
ALCEMISTE
Generic name
LIDOCAINE HCL
Manufacturer
Price Team Ventures, LLC
Product type
HUMAN OTC DRUG
SPL set ID
4383faaa-49cf-47b7-83a6-c2a94b6ff9b5
SPL ID
3e130768-8805-93a4-e063-6294a90a5bfd
Version
1
Effective date
2025-09-05
Source export date
2026-11-06
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/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:01:09
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 1. For external use only 2. Avoid contact with the eyes 3. Stop use and consult a doctor if : Condition worsens or symptoms persist for more than 7 days Symptoms clear up and occur again within a few days Avoid excessive use, especially on raw or blistered skin. Do not exceed the recommended daily dosage unless advised by a doctor. Do not use on wounds or damaged skin. Keep out of reach of children . If swallowed, seek immediate medical attention or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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