MAXOCAINE PAIN RELIEVING ROLL-ON

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 PAIN RELIEVING ROLL-ON
Generic name: LIDOCAINE HYDROCHLORIDE, MENTHOL
Manufacturer: Prime Commerce, LLC
Product type: HUMAN OTC DRUG
SPL set ID: c263d5f2-89b9-4dfd-91c8-f894e5f956c9
SPL ID: 09dc681e-2348-4213-e063-6394a90a41e1
Version: 3
Effective date: 2023-11-11
Source export date: 2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:51:55

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		M017	openfda.application_number
brand name		MAXOCAINE PAIN RELIEVING ROLL-ON	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE, MENTHOL	openfda.generic_name
manufacturer name		Prime Commerce, LLC	openfda.manufacturer_name
ndc	package	72188-170-03	openfda.package_ndc
ndc	product	72188-170	openfda.product_ndc
ndc11	package	72188017003	derived:openfda.package_ndc
rxcui		2002008	openfda.rxcui
spl id		09dc681e-2348-4213-e063-6394a90a41e1	id
spl set id		c263d5f2-89b9-4dfd-91c8-f894e5f956c9	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 Avoid contact with eyes. If symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not apply to wounds or damaged skin. Do not bandage tightly. If pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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