MAXOCAINE Lidocaine Hemp Oil Topical Analgesic

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
MAXOCAINE Lidocaine Hemp Oil Topical Analgesic
Generic name
LIDOCAINE HYDROCHLORIDE
Manufacturer
Prime Commerce, LLC
Product type
HUMAN OTC DRUG
SPL set ID
28ed2149-38d2-4062-8442-990a98a69cfc
SPL ID
09dc64a4-8591-ddca-e063-6294a90ab8f1
Version
2
Effective date
2023-11-11
Source export date
2026-10-27
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:12:09
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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. When using this product avoid contact with the eyes. Stop use and ask a doctor if condition worsens, or if symptoms persist for 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. If pregnant or breast-feeding. ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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