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Zylotrol Maximum Pain drug information

LIDOCAINE 4%, MENTHOL 1%
Whitestone Products LLC · TOPICAL

Product NDC: 81902-104

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameLIDOCAINE 4%, MENTHOL 1%
Labeler / manufacturerWhitestone Products LLC
RouteTOPICAL
Drug classAmide Local Anesthetic / Antiarrhythmic
Product NDC81902-104
Label effective date2026-08-21

Official product label reference

Zylotrol Maximum Pain — Whitestone Products LLC

This page contains 13 source sections for LIDOCAINE 4%, MENTHOL 1%, topical route. Label set a80efad7-1d8b-4d8b-8c97-373174ce89ca, version 3.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses For the temporary relief of pain.

Purpose

Purposes Topical Analgesic Topical Analgesic
Dosage and administration — label text
Directions Adult and children 12 years of age and over: Clean and dry affected area Remove film from patch and apply to the skin (see illustration) Apply 1 patch at a time to affected area, not more than 3 to 4 times daily Remove patch from the skin after at most 8-hour application Children under 12 years of age: Consult a doctor
Warnings
Warnings For external use only
Active ingredient
Active Ingredients Lidocaine 4% Menthol 1%
Do not use
Do not use: More than 1 patch at a time On wounds or damaged skin If you are allergic to any ingredients of this product
While using this medicine
When using this product: Use only as directed Avoid contact with the eyes, mucous membranes or rashes Do not bandage tightly
When to stop use and seek help
Stop use and ask a doctor if: Localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering Condition worsen Symptoms persist for more than 7 days Symptoms clear up and occur again within a few days
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Storage and handling
Other information Store at 68-77℉ (20-25℃) Store in a cool dry place away from direct sunlight
Inactive ingredient
Inactive Ingredients Water, Glycerin, Polyacrylic Acid, Propylene Glycol, Sodium Polyacrylate, Polysorbate 80, Mineral oil, Polyvinylpyrrolidone K90, Hydroxyacetophenone, L(+)-Tartaric Acid, Dihydroxyaluminium Aminoacetate, Edetate Disodium, Kaolin, Titanium Dioxide
Questions
Questions? (888) 726-7848

Official sources and product identifiers

Substances listed: MENTHOL, LIDOCAINE

RxNorm identifiers: 1249758

Package NDC codes

81902-104-15

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.