Medical emergency?Emergency? Call 911. Nearest emergency roomsNearest ERs

Over-the-counter medicine · no prescription needed

Capsaicin, lidocaine hydrochloride, menthol, (+)- and methyl salicylate

Purpose on the label: counterirritant anesthetic 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 Capsaicin, lidocaine hydrochloride, menthol, (+)- and methyl salicylate used for?
The Drug Facts label of LidoPro Pain Relief (Preferred Pharmaceuticals Inc.) lists these uses: For the temporary relief of joint pain and muscle pain associated with; arthritis; simple backache; muscle sprains; muscle strains.
Do I need a prescription for Capsaicin, lidocaine hydrochloride, menthol, (+)- and methyl salicylate?
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 Capsaicin, lidocaine hydrochloride, menthol, (+)- and methyl salicylate 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.

LidoPro Pain Relief · Preferred Pharmaceuticals Inc.

Capsaicin 0.0325 mg/100 mg · Lidocaine hydrochloride 4 mg/100 mg · Menthol, (+)- 10 mg/100 mg · Methyl salicylate 27.5 mg/100 mg, ointment (transdermal)

Active ingredient

• Capsicum annum fruit extract (capsaicin) • Lidocaine HCL • Menthol • Methyl Salicylate

Purpose

• counterirritant • anesthetic • analgesic

Uses

For the temporary relief of joint pain and muscle pain associated with:

  • arthritis
  • simple backache
  • muscle sprains
  • muscle strains

Warnings

For external use only.

Do not use

  • on damaged, irritated or infected skin
  • with a bandage or heating pad
  • if you are allergic to any ingredients in this product

When using this product

avoid contact with the eyes and mucous membranes Stop use and ask doctor if

  • condition worsens
  • excessive skin
  • irritation develops
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within 3 days

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

If ingested, seek medical help or contact a Poison Control Center immediately. Flammable Keep away from excessive heat or open flame.

Directions

Adults and children 12 years of age and older:

  • clean and dry the affected area
  • apply product directly to skin, up to 4 times daily
  • wash hands immediately after use Children under 12 years of age: Consult physician.

Other information

Flammable Keep away from excessive heat or open flame. Other information

  • Store in a cool, dry place with lid tightly closed
  • if the tamper-evident foil seal is not intact, do not use

Inactive ingredients

allantoin, aloe barbadensis leaf juice, ammonium acryloyldimethyltaurate/vp copolymer, cetyl alcohol, chamomilla recutita matricaria flower extract, dimethicone, disodium EDTA, ethylhexylglycerin, glycerin, glyceryl stearate, inulin lauryl carbamate, PEG-100 stearate, phenoxyethanol, stearic acid, triethanolamine, water

Questions?

(800) 224-2048 or info@clinicpharma.com Relabeled By: Preferred Pharmaceuticals Inc. NDC 68788-8833-9

— FDA label of LidoPro Pain Relief, Preferred Pharmaceuticals Inc., effective February 21, 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.

Capsaicin 0.0325 mg/100 mg · Lidocaine hydrochloride 4 mg/100 mg · Menthol, (+)- 10 mg/100 mg · Methyl salicylate 27.5 mg/100 mg · ointment (transdermal) · 3 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
LidoPro Pain Relief Advanced Rx of Tennessee, LLC DailyMed
LidoPro Pain Relief Clinic Pharma DailyMed
LidoPro Pain Relief Preferred Pharmaceuticals Inc. 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.

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.

Report an error → · Information for medicine makers