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Zylotrol maximum pain patch - Medication Information

Product NDC Code 81902-101
Drug Name

Zylotrol maximum pain patch

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine 4 g/100g
Menthol, unspecified form 1 g/100g
Route TOPICAL
Dosage Form PATCH
RxCUI drug identifier 1249758
Application Number 505G(a)(3)
Labeler Name Whitestone Products LLC
Packages
Package NDC Code Description
81902-101-15 15 patch in 1 box (81902-101-15) / 4 g in 1 patch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Lidocaine 4% Menthol 1%

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 2 years of age and older: Apply to affected area not more than 3 to 4 times a daily. Children under 2 years of age: consult a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
polyacrylamide, vinol, sodium polyacrylate; acrylate polymerization; purified 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 For the temporary relief of pain.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Zylotrol Maximum Pain Patch Lidocaine 4%, Menthol 1% WATER ACRYLATES CROSSPOLYMER-6 POLYACRYLAMIDE (10000 MW) SODIUM POLYACRYLATE (2500000 MW) ETHENYL LIDOCAINE LIDOCAINE MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM

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.
box

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
condition worsens, or if symtoms persist for more than 7 days or clear up and occur again within a few days.

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
in large quantities, particularly over raw surfaces, or blistered areas.

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

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Store at 20-25oC (68-77oF) and protect from moisture.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? (310) 320-0100

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
Avoid contact with eyes.

Pregnancy or breast feeding

Pregnancy or Breast feeding
ask a health professional before use.

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.
For external use only not intended for ingestion.

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