Foot

Menthol · Cream · Topical

Over the counter

Active ingredient

Drug Facts Active Ingredient Menthol 1.25%

Purpose

Purpose Topical analgesic

Uses

Uses For temporary relief of minor aches and pains

Warnings

Warnings For external use only Avoid contact with eyes If condition worsens, or if symptoms persist for more than 7 days or cler up and occur again within a few days,, discontinue use of this product and consult a doctor. If pregnant or breast-feeding, ask a health professional before use.

Stop use and ask a doctor

If condition worsens, or if symptoms persist for more than 7 days or cler up and occur again within a few days,, discontinue use of this product and consult a doctor.

Pregnancy or breast-feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions Adults and children 2 years of age and over: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age consult a doctor.

Inactive ingredients

Inactive Ingredients Arnica montana flower extract, cetyl palmitate, ethylhexylglycerin, glycerin, glyceryl stearate, jojoba (Buxus chinensis) oil, peppermint (mentha piperita) oil, phenoxyethanol, sodium citrate, stearic acid, sweet almond (Prunus amydgalus dulcis) oil, tea tree (Melaleuca alternifolia) oil, tocopherol (Vitamin E), water

Questions?

Questions? Call (866) 419-3567 Monday through Friday 8:00am - 2:00pm ET

Label text from the FDA structured product label by Smith Amish, LLC (revised Dec 12, 2025). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Menthol in 1 product

Foot NDC products (1)

NDC	Strength & form	Labeler	Type
72609-703	Menthol 1.25 g/100g Cream	Smith Amish, LLC	OTC MONOGRAPH DRUG

Frequently asked questions

What is Foot used for?

Uses For temporary relief of minor aches and pains

Who makes Foot?

Foot is listed by 1 labeler in the FDA NDC directory, including Smith Amish, LLC.