LenzaPro Flex LIDOCAINE MENTHOL SOLA PHARMACEUTICALS FDA Approved Uses: For the temporary relief of pain
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Substance Lidocaine
Route
TOPICAL
Applications
M017
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Active ingredients: Lidocaine HCL 4% Menthol 4%
Inactive Ingredients
Other Ingredients: Acrylic Adhesive
Strengths
4 %
Treats Conditions
Uses For The Temporary Relief Of Pain
Pill Appearance
Shape: rectangle

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UPC
0070512013157
UNII
98PI200987 L7T10EIP3A
Packaging

Questions or comments? 866-747-7365 Manufactured For: SOLA Pharmaceuticals LLC Baton Rouge, LA 70810 NDC: 70512-013-15 QTY: 15 Articulated patches (5 per Resealable Pouch) x 3 Lenzapro Flex

Package Descriptions
  • Questions or comments? 866-747-7365 Manufactured For: SOLA Pharmaceuticals LLC Baton Rouge, LA 70810 NDC: 70512-013-15 QTY: 15 Articulated patches (5 per Resealable Pouch) x 3 Lenzapro Flex

Overview

Uses: For the temporary relief of pain

Indications & Usage

Uses: For the temporary relief of pain

Dosage & Administration

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

Warnings & Precautions
Warnings: For external use
Purpose

Purpose: Topical Anesthetic

Do Not Use

Do not use: More than 1 patch on your body at a time or on cut, iritated or swollen skin. On puncture wounds For more than 1 week without consulting a doctor

When Using

When using this product: Use only as directed. Read and follow all directions and warnings on this label. Rare cases of serious burns have been reported with products of this type. Do not apply to wounds or damaged, broken or irritated skin. Do not allow contact with the eyes and mucous membranes. Do not bandage tightly or apply local heat (such as heating pads) to the area of use. Do not use at the same time as other topical analgesics. Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

Stop Use & Ask a Doctor

Stop use and ask a doctor if: Condition worsens Redness is present Irritation developes Symptoms persist for more than 7 days or clear up and occur again within a few days. You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.

Keep Out of Reach of Children

Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.


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