Numotizine

Menthol · Ointment · Topical

Over the counter

Active ingredient

Active Ingredients Menthol 1.25%

Purpose

Purpose Topical Analgesic

Uses

Uses For use as a topical analgesic Provides temporary relief of muscle pain, soreness and stiffness Temporary pain relief on strains, sprains, ligament and tendon injuries Arthritis

Warnings

Warnings: For external use only. Use only as directed. Avoid contact with eyes and mucous memebranes. Do not apply to irritated or broken skin or to large areas of the body.

Stop use and ask a doctor

Stop use and ask a doctor if Excessive irritation of the skin occurs. Persistent swellings.

Keep out of reach of children

Keep out of the reach of children

Directions

Directions Stir in any liquid at top of jar. Keep sealed when not in use. Spread 1/8" to 1/4" of ointment to the skin. Cover the ointment with a cloth or bandage to protect clothing. Remove with warm water before totally dry (usually 8 to 12 hours). Application may be repeated every 12 hours as needed.

Inactive ingredients

Inactive ingredients Clay, Color, Fragrance of Guaiacol, Methyl Guaiacol and Oil of Wintergreen, Polyols.

Label text from the FDA structured product label by Hobart Laboratories, Inc. (revised Oct 20, 2023). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Numotizine NDC products (1)

NDCStrength & formLabelerType
10546-100Menthol 1.25 g/100g
Ointment
Hobart Laboratories, Inc.OTC MONOGRAPH DRUG

Frequently asked questions

What is Numotizine used for?

Uses For use as a topical analgesic Provides temporary relief of muscle pain, soreness and stiffness Temporary pain relief on strains, sprains, ligament and tendon injuries Arthritis

Who makes Numotizine?

Numotizine is listed by 1 labeler in the FDA NDC directory, including Hobart Laboratories, Inc..