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OTC products · Product label record

MAXIMUM STRENGTH Lidocaine Plus Menthol drug information

LIDOCAINE, MENTHOL
ARMY AND AIR FORCE EXCHANGE SERVICE · TOPICAL

Product NDC: 55301-912

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Generic nameLIDOCAINE, MENTHOL
Labeler / manufacturerARMY AND AIR FORCE EXCHANGE SERVICE
RouteTOPICAL
Drug classAmide Local Anesthetic / Antiarrhythmic
Product NDC55301-912
Label effective date2026-08-20

Official product label reference

MAXIMUM STRENGTH Lidocaine Plus Menthol — ARMY AND AIR FORCE EXCHANGE SERVICE

This page contains 13 source sections for LIDOCAINE, MENTHOL, topical route. Label set 60f72061-d264-424e-b396-5a609076d352, 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 Temporary relief of minor pain

Purpose

Topical Anesthetic
Dosage and administration — label text
DIRECTIONS Adults and children 12 years of age and over: Clean and dry affected area. Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Use one patch for up to 12 hours. Discard after single use. Children under 12 years of age: consult a physician.
Warnings
WARNINGS For External use only. Use only as directed. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. ■ More than one patch on your body at a time ■ On cut, irritated or swollen skin ■ On puncture wounds ■ For more than one week without consulting a doctor ■ If you are allergic to any active or inactive ingredients ■ If pouch is damaged or opened. If pregnant or breast feeding Contact a physician prior to use. WHEN USING: ■ Use only as directed ■ Read and follow all directions and warnings on this carton ■ Do not allow contact with the eyes ■ Do not use at the same time as other topical analgesics ■ Do not bandage tightly or apply local heat (such as heating pads) to the area of use ■ Do not microwave ■ 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 and consult a doctor if ■ Condition worsens ■ Redness is present ■ Irritation develops ■ 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.
Unclassified section
Drug Facts
Active ingredient
Lidocaine 4% Topical Anesthetic Menthol 1% Topical Anesthetic
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Do not use
■ More than one patch on your body at a time ■ On cut, irritated or swollen skin ■ On puncture wounds ■ For more than one week without consulting a doctor ■ If you are allergic to any active or inactive ingredients ■ If pouch is damaged or opened.
Pregnancy or breast feeding
If pregnant or breast feeding Contact a physician prior to use.
While using this medicine
WHEN USING: ■ Use only as directed ■ Read and follow all directions and warnings on this carton ■ Do not allow contact with the eyes ■ Do not use at the same time as other topical analgesics ■ Do not bandage tightly or apply local heat (such as heating pads) to the area of use ■ Do not microwave ■ 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.
When to stop use and seek help
Stop use and consult a doctor if ■ Condition worsens ■ Redness is present ■ Irritation develops ■ 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.
Inactive ingredient
INACTIVE INGREDIENTS carboxymethylcellulose sodium, dihydroxyaluminum aminoacetate, ethylhexylglycerin, glycerin, iodopropynyl butylcarbamate, kaolin, petrolatum, phenoxyethanol, polyacrylic acid, polysorbate 80, povidone, propylene glycol, sodium polyacrylate, tartaric acid, titanium dioxide, water
Storage and handling
Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture.

Official sources and product identifiers

Substances listed: LIDOCAINE, MENTHOL, UNSPECIFIED FORM

RxNorm identifiers: 1249758

Package NDC codes

55301-912-05

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.