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Theralast Maximum Strength Pain Relief Gel

Dosage form
GEL
Labeler
SKIN SHERPA NORTH AMERICA LLC
Label updated
2022-03-21
Retrieved
2026-09-07
Active ingredients
MENTHOL
View original label and images on DailyMed ↗
Active ingredient

Menthol 4%

Purpose

Topical analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with:

  • simple backache
  • strains
  • sprains
  • bruises
  • arthritis
Warnings

For external use only.

Do not use

  • on large areas of the body
  • with other ointments, creams, sprays or liniments
  • with heating pad

Ask a doctor before use if you have

sensitive skin or redness over the affected area

When using this product

  • avoid contact with eyes or mucus membranes
  • do not apply to wounds or damaged skin
  • do not bandage
  • wash hands after use

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • excessive skin irritation occurs

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children.

If accidentally ingested, get medical help or contact a Poison Control Center immediately.

Directions
  • Use only as directed
  • Adults and children over 12 years: apply to affected area not more than 4 times daily.
  • Children under 12 years of age: Consult physician.
Other information

Store in cool dry place

Inactive ingredients

Alcohol Denat., Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Butylene Glycol, Diethyl Azelate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isopropyl Alcohol, Methyl Hydroxypropyl Cellulose, Polyacrylate Crosspolymer 6, Polysorbate 20, Water

Questions?

1-833-499-0932 or theralast.com

Company Information

Distributed by Skin Sherpa North America, LLC, 18756 Stone Oak Parkway, Ste. 200San Antonio, TX 78258

www.theralast.com

Product Packaging

[Image in the official label — see DailyMed source]

DailyMed Set ID: d8a63dc0-9e21-0bcd-e053-2a95a90a71bd · Version 2
NDC: 80967-003