FDA.reportPublic FDA data

Lidocaine HCI

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
Lidocaine HCI
Generic name
LIDOCAINE HCI
Manufacturer
Trifluent Pharma, LLC
Product type
HUMAN OTC DRUG
SPL set ID
47f7f06b-720e-eeec-e063-6294a90ae823
SPL ID
47f7f06b-720f-eeec-e063-6294a90ae823
Version
1
Effective date
2026-01-09
Source export date
2026-08-01
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/5cbbf4af8f4e275ec50931155b30ffa7322568b9af8a1c936a47f6d6774862fd/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:01:38
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 Do not use in large quantities, particularly over raw surfaces or blistered areas. 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, discontinue use or this product and consult a doctor. If pregnant or breast-feeding , ask a health professional before use. .