LenzaPro Flex Patch

Manufacturer: Direct_Rx
Effective date: 2023-08-16
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 21:27:15

Label at a glance#

ProductLenzaPro Flex Path

Active ingredientMENTHOL, LIDOCAINE

Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Uses:

For the temporary relief of pain

WARNINGS SECTION

Warnings:

For external use

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children over 12 years:

Clean and dry the affected area.
Open pouch and remove one patch.
Remove the protective film from the patch and apply patch to the affected area.
Reseal pouch containing unused patches after each use.
Use 1 patch for up to 12 hours.

Children 12 years or younger:

Ask a doctor

OTC - ACTIVE INGREDIENT SECTION

Active ingredients:

Lidocaine HCL 4%

Menthol 4%

OTC - PURPOSE SECTION

Purpose:

Topical Anesthetic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health care professional before use.

INACTIVE INGREDIENT SECTION

Other Ingredients:

Acrylic Adhesive

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

72189-361-15

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72189-361-15	EA - Each	72189-361	5ef68cbf-41b7-4e00-ac57-26224a9daeb9	1	2022-08-04
70512-013-15	EA - Each	70512-013	2a3dd89e-8aed-4d3a-b817-bba1f2a0e083	1	2021-04-08

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

LenzaPro Flex Path
MENTHOL
LIDOCAINE
ACRYLIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72189-361	72189-361-15
70512-013

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
LIDOCAINE	98PI200987	ACTIB
ACRYLIC ACID	J94PBK7X8S	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
LenzaPro Flex	LIDOCAINE/MENTHOL	SOLA Pharmaceuticals	ba498f1d-460b-f4e6-e053-2995a90a5755	2025-12-08	Warnings	Exact identifier ndc (product): 70512-013
074b730e-ba78-c0de-e063-6294a90a964f			e20b3c53-d18c-9ddb-e053-2a95a90ad6f4	2023-10-09	Warnings	Exact identifier spl set id: e20b3c53-d18c-9ddb-e053-2a95a90ad6f4

Reported adverse events (FAERS/openFDA)#

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