Medicine guide

Pain Relief Gel Roll On

40 g/L · Gel

  • Available without prescription
Active substance
Menthol
Made by
Trifecta Pharmaceuticals USA

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

At a glance

Quoted from the official label · 2026-04-30

What it is

Topical Analgesic

Used for
  • And use Temporarily relieves minor aches and pains of muscles and joints associated with simple backache arthritis strains bruises sprains
Warning

For external use only. Flammable Keep away from excessive heat or open flames.

All warnings ↓
Good to know
  • Sold without a prescription
  • FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-03
849other products contain Menthol — compare makers, forms and strengths

Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed

What it is for

  • and use Temporarily relieves minor aches and pains of muscles and joints associated with simple backache arthritis strains bruises sprains

From the official label · 2026-04-30 · DailyMed

How to take it

These directions are for this exact strength and form. Another one is different.

  • Adults and
  • children 2 years of age and older:
  • rub a thin film over affected area not more than 3 to 4 times daily.
  • Children under 2 years of age:
  • ask a doctor Wash hands after use with cold water.

Quoted from the official label, section “Dosage & Administration”.

Stop and get help if

  • and Ask Doctor if
  • Stop use and ask doctor
  • if you experience pain, swelling or blistering of the skin if condition worsens or
  • if symptoms persist for more than 7 days or clear up and occur again within a few days arthritic pain persists for more than 10 days or redness is present, or in conditions affecting
  • children under 12 years of age.

Quoted from the official label, section “OTC — Stop Use”.

Other warnings

For external use only. Flammable Keep away from excessive heat or open flames.

Quoted from the official label, section “Warnings”.

Pregnancy and breastfeeding

If Pregnant or breast feeding If Pregnant or breast feeding as a doctor before use.

Quoted from the official label, section “OTC — Pregnancy or Breast Feeding”.

Keep away from children

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

Quoted from the official label, section “OTC — Keep Out of Reach of Children”.

How to store it

Store at 20° to 25°C (68° to 77°F) Store in cool dry place away from direct sunlight

Quoted from the official label, section “Storage and Handling”.

What kind of medicine it is

Topical Analgesic

Quoted from the official label, section “OTC — Purpose”.

Other ingredients

Relevant if you react to a dye, a preservative, lactose or gluten.

Alcohol, Aloe Vera extract, Arnica Montana Flower extract, Boswellia carteril resin extract, Camellia sinesis leaf extract, Camphor, Carbomer, FD&C Blue 1, FD&C Yellow 5, Glycerin, Ilex parguariensis leaf extract, Isopropyl myristate, Silica, Triethanolamine, Vitamin E, Water.

Quoted from the official label, section “Inactive Ingredients”.

Questions about this product

Call 1-888-296-9067

Quoted from the official label, section “OTC — Questions”.

Ingredients people check for

Lactose, gluten, dyes, sugars and other ingredients that matter with an allergy, intolerance or diet — as this product’s FDA label lists them.

  • Colour dyesFD&C Blue 1; FD&C Yellow 5Some people react to dyes such as tartrazine (Yellow 5) or carmine.
  • Alcohol (ethanol)AlcoholMatters for children, in pregnancy, in recovery and with some medicines.

Quoted from the FDA label. A label that does not name an ingredient is not a guarantee that the product is free of it, and formulations change. With an allergy, check the pack and ask a pharmacist.

Details

Made byTrifecta Pharmaceuticals USA
Active substanceMenthol
Strength40 g/L
FormGel
RouteTopical
Packs1 BOTTLE in 1 BOX / .074 L in 1 BOTTLE · 3 BOTTLE in 1 BOX / .074 L in 1 BOTTLE
NDC69396-184

Source: NDC Directory · 2026-09-13 · not reviewed by a clinician

Source: US Food and Drug Administration, NDC Directory. Reuse terms: US government work (FDA).

Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.