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Lidocanna - Medication Information

Product NDC Code 79643-001
Drug Name

Lidocanna

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine 4 g/100g
Route TOPICAL
Dosage Form PATCH
Application Number M017
Labeler Name PHARMACURE LLC
Packages
Package NDC Code Description
79643-001-01 10 patch in 1 box (79643-001-01) / 14 g in 1 patch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Lidocaine 4%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Adults and children 12 years and over: apply 1 to 2 patches to the affected area of intact skin. Lidocanna should be removed after 12 hours of continuous use and remain off for at least 12 hours.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Cannabidiol, eucalyptus oil, glycerin, glycol dihydroxy aluminum, lavender oil, peppermint oil, polyacrylic acid, propyl p-hydroxybenzoate, propylene glycol, tartaric acid, water

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Temporarily relieves mild to moderate aches and pains of muscles and joints associated with muscle soreness, strains, sprains, arthritis, simple backache, muscle stiffness, bruises.

Purpose

Information about the drug product’s indications for use.
Purpose Topical Anesthetic

Spl product data elements

Usually a list of ingredients in a drug product.
Lidocanna LIDOCAINE WATER CANNABIDIOL EUCALYPTUS OIL GLYCERIN LAVENDER OIL PEPPERMINT OIL POLYACRYLIC ACID (250000 MW) PROPYLPARABEN PROPYLENE GLYCOL TARTARIC ACID LIDOCAINE LIDOCAINE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Product Label image description

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If product is put in mouth, get medical help of contact a Poison Control Center right away. Package is not child resistant. Dispose of the used patches by folding sticky ends together.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Some individuals may not experience pain relief until several minutes or hours after applying the patch. Store in a cool, dry place. Protect the product from excessive moisture or sunlight. Store at 67-77°F (19-25°C).

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Do not use on the face or rashes, on wounds or damaged skin, in the eyes, mouth, or other mucous membranes, on genitals, with a heating pad, any patch from a pouch that has been opened for 7 or more days. Ask a doctor before use if you are allergic to topical products, you are taking a diuretic, you have high blood pressure, heart disease, kidney disease, or you are pregnant. When using this product wash hands after applying or removing patch. Avoid contact with eyes. If eye contact occurs, rinse thoroughly with water. Stop use and consult your physician if rash, irritation, or itching develops, or condition worsens. If pregnant or breastfeeding, ask a doctor before use while breastfeeding and during the first 6 months of pregnancy. Do not use during the last 3 months of pregnancy because it may cause problems in the unborn child or complications during delivery. For external use only

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API