NDC 70512-013 Lenzapro Flex

Lidocaine/menthol

NDC Product Code 70512-013

NDC CODE: 70512-013

Proprietary Name: Lenzapro Flex What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Lidocaine/menthol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to relieve nerve pain after shingles (infection with the herpes zoster virus). This type of pain is called post-herpetic neuralgia. Lidocaine helps to reduce sharp/burning/aching pain as well as discomfort caused by skin areas that are overly sensitive to touch. Lidocaine belongs to a class of drugs known as local anesthetics. It works by causing a temporary loss of feeling in the area where you apply the patch.

NDC Code Structure

  • 70512 - Sola Pharmaceuticals

NDC 70512-013-15

Package Description: 3 POUCH in 1 BOX > 1 g in 1 POUCH

NDC Product Information

Lenzapro Flex with NDC 70512-013 is a a human over the counter drug product labeled by Sola Pharmaceuticals. The generic name of Lenzapro Flex is lidocaine/menthol. The product's dosage form is patch and is administered via topical form.

Labeler Name: Sola Pharmaceuticals

Dosage Form: Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Lenzapro Flex Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • MENTHOL 40 mg/g
  • LIDOCAINE 40 mg/g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ACRYLIC ACID (UNII: J94PBK7X8S)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Sola Pharmaceuticals
Labeler Code: 70512
FDA Application Number: part348 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 02-01-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Lenzapro Flex Product Label Images

Lenzapro Flex Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active ingredients:Lidocaine HCL 4%Menthol 4%

Otc - Purpose

Purpose:Topical Anesthetic

Indications & Usage

Uses:For the temporary relief of pain

Warnings

Warnings:For external use

Otc - 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 woundsFor more than 1 week without consulting a doctor

Otc - 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.

Otc - Stop Use

  • Stop use and ask a doctor if:Condition worsensRedness is presentIrritation developesSymptoms 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.

Otc - Pregnancy Or Breast Feeding

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

Otc - 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.

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

Other Safety Information

  • Other Information:Avoid storing product in direct sunlightProtect product from excessive mositure

Inactive Ingredient

Other Ingredients:Acrylic Adhesive

* Please review the disclaimer below.