Lidochill(TM) Gel

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: Lidochill(TM) Gel
Generic name: LIDOCAINE HCL 4%, MENTHOL 1%
Manufacturer: PureTek Corporation
Product type: HUMAN OTC DRUG
SPL set ID: d2a9aeb6-8a94-49e7-ab46-84403560b6c8
SPL ID: 3e4f5664-2734-582d-e063-6294a90a41ed
Version: 5
Effective date: 2025-09-08
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:54:22

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Lidochill(TM) Gel	openfda.brand_name
generic name		LIDOCAINE HCL 4%, MENTHOL 1%	openfda.generic_name
manufacturer name		PureTek Corporation	openfda.manufacturer_name
ndc	package	59088-240-16	openfda.package_ndc
ndc	product	59088-240	openfda.product_ndc
ndc11	package	59088024016	derived:openfda.package_ndc
rxcui		1373137	openfda.rxcui
spl id		3e4f5664-2734-582d-e063-6294a90a41ed	id
spl set id		d2a9aeb6-8a94-49e7-ab46-84403560b6c8	set_id
unii		L7T10EIP3A	openfda.unii
unii		V13007Z41A	openfda.unii

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 apply to wounds or damaged skin ■ Do not bandage tightly When using this product ■ Avoid contact with the eyes Stop use and ask a doctor if 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. 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.