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Over-the-counter medicine · no prescription needed

Levomenthol and lidocaine

Purpose on the label: Lidocaine Topical analgesic Menthol Topical analgesic

Pain relief on the skin

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Levomenthol and lidocaine used for?
The Drug Facts label of Satohap Lidocaine 4% Menthol 1% Pain Relieving Cream (Sato Pharmaceutical Co., Ltd.) lists these uses: For temporary relief of pain.
Do I need a prescription for Levomenthol and lidocaine?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Levomenthol and lidocaine been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

Satohap Lidocaine 4% Menthol 1% Pain Relieving Cream · Sato Pharmaceutical Co., Ltd.

Levomenthol 1% · Lidocaine 4%, cream (topical)

Active ingredient

Lidocaine 4% Menthol 1%

Purpose

Lidocaine Topical analgesic Menthol Topical analgesic

Uses

For temporary relief of pain

Warnings

For external use only

Do not use

in large quantities, particularly over raw surfaces or blistered areas

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days a rash or irritation develops

Keep out of reach of children

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

Directions

adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times dailly children under 12 years of age: do not use, ask a doctor

Other information

protect product from excessive moisture avoid storing in direct sunlight store with lid tightly closed

Inactive ingredients

benzyl alcohol, butylene glycol, carbomer homopolymer (type C), isopropyl myristate, polyoxyl 40 hydrogenated castor oil, sodium hydroxide, water

— FDA label of Satohap Lidocaine 4% Menthol 1% Pain Relieving Cream, Sato Pharmaceutical Co., Ltd., effective December 30, 2024. See the official label on DailyMed →

Maximum Strenght Lidocaine plus Menthol Pain Relief Patch · Rite Aid Corporation

Levomenthol 1% · Lidocaine 4%, patch (topical)

Active ingredient

Lidocaine 4.0% . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Topical Anesthetic Menthol 1.0% . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Topical Anesthetic

Purpose

Uses Temporarily relieves minor pain.

Uses

Temporarily relieves minor pain.

Warnings

For external use only. 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.

When using this product

  • 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
  • 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.

If pregnant or breastfeeding

ask a health professional before use.

Keep out of reach of children

and pets. If swallowed, get medical help or contact a Poison Control Center 800-222-1222 right away.

Directions

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 patch after single use.
  • Children under 12 years of age: consult a physician.

Other information

Other Safety Information Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture.

Inactive ingredients

Carboxymethylcellulose sodium, Dihydroxyaluminum Aminoacetate, Glycerin, iodopropynyl butylcarbamate, Kaolin, petrolatum, Phenoxyethanol, polyacrylic acid, Polysorbate 80, Povidone, Propylene Glycol, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Water, 3-(2-ethylhexyloxy)propane-1,2-diol

— FDA label of Maximum Strenght Lidocaine plus Menthol Pain Relief Patch, Rite Aid Corporation, effective December 18, 2024. See the official label on DailyMed →

AUVON Lidocaine Menthol Pain Relief Patch · Shenzhen Yuwen E-Commerce Co., Ltd.

Levomenthol 100 mg · Lidocaine 400 mg, patch (topical)

Active ingredient

Lidocaine 4% Menthol 1%

Purpose

Topical anesthetic

Uses

for the temporary pain relief

Warnings

For external use only If you are allergic to the listed ingredients If you are pregnent or breast feeding If you are under 12 years of age On wounds, cuts, damaged/broken/irritated skin On eyes or mucous membranes With heating pads/devices or wrap with a bandage With other topical analgesics If the package arrives damaged or opened.

  • Read and follow all directions and warnings on this label
  • avoid contact with the eyes and mucous membranes
  • rare cases of serious burns have been reported with products of this type
  • a transient burning sensation may occur upon application but generally disappears in several days
  • 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. You are experiencing pain, swelling or blistering Redness is persent or irritation develops Symptoms persist for more than 7 days or clear up and occur again within a few days Children under 12years of age: do not use, consult a doctor.

Directions

  • Clean and dry the patch application area (no wound or hair), pull to separate the film, peel off one side of the film, apply the exposed patch to the skin, peel off the
  • Do not repeatedly use or repeatedly reapply the patch as far as possible
  • Cut first if if used on joints
  • Use in te affected area no more than 4 times daily
  • Wash hands with cool water after use

Inactive ingredients

Dihydroxyaluminum Aminoacetate Edetate Disodium Glycerin Hydroxyacetophenone Kaolin L(+)-Tartaric Acid Mineral oil Polysorbate 80 Polyacrylic Acid Polyvinylpyrrolidone K90 Propylene Glycol Sodium Polyacrylate Titanium Dioxide Water

— FDA label of AUVON Lidocaine Menthol Pain Relief Patch, Shenzhen Yuwen E-Commerce Co., Ltd., effective March 20, 2025. See the official label on DailyMed →

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

Same medicine, other brands

Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Levomenthol 1% · Lidocaine 4% · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Satohap Lidocaine 4% Menthol 1% Pain Relieving Cream Sato Pharmaceutical Co., Ltd. DailyMed
Levomenthol 1% · Lidocaine 4% · patch (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Maximum Strenght Lidocaine plus Menthol Pain Relief Patch Rite Aid Corporation DailyMed
Levomenthol 100 mg · Lidocaine 400 mg · patch (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
AUVON Lidocaine Menthol Pain Relief Patch Shenzhen Yuwen E-Commerce Co., Ltd. DailyMed

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

  • Sato Pharmaceutical Co., Ltd.1 product
  • Rite Aid Corporation1 product
  • Shenzhen Yuwen E-Commerce Co., Ltd.1 product

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

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