Medicine guide

Pain Relief Gel-Roll On

40 g/L · Gel

  • Available without prescription
  • Amide Local Anesthetic
Active substance
Lidocaine
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 · 2026-05-14

The FDA lists a current shortage of lidocaine

Not necessarily this product — shortages are reported per presentation. Your pharmacy will know. · Updated 2026-09-22 FDA drug shortages

What it is

Topical Analgesic

Used for
  • And use Temporarily relieves minor pain.
Do not take it if

Do Not Use On large areas of the body or on cut, irritatied or swollen skin on puncture wounds for more than one week without consulting a doctor

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 2026-10-02
410other products contain Lidocaine — 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 pain.

From the official label · 2026-05-14 · DailyMed

How it works

From the US prescribing label for the same active substance (LIDOCAINE). It describes the substance, not this exact product.

Lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses, thereby effecting local anesthetic action.

Half-life1.5–2.0 h
Mostly cleared after≈ 8.8 hfive half-lives — our arithmetic
How the body breaks it down

Lidocaine is metabolized rapidly by the liver, and metabolites and unchanged drug are excreted by the kidneys.

Quoted from the prescribing label, sections “Mechanism of Action” and “Pharmacokinetics”. DailyMed · 2026-08-31

Do not take it if

Do Not Use On large areas of the body or on cut, irritatied or swollen skin on puncture wounds for more than one week without consulting a doctor

Quoted from the official label, section “OTC — Do Not Use”.

How to take it

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

  • Adults and children over 12 years:
  • apply a thin layer to the affected area not more than 3 to 4 times daily. Children 12 years or younger:
  • ask a doctor

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

Stop and get help if

  • and Ask Doctor if
  • Stop use and ask doctor if Condition worsens Redness is present irritation devlops symptoms persisit for more than 7 days or clear up and occur again within a few days

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

Other warnings

  • Section For External Use Only Flammable - keep away from fire or flames.
  • When using this product use only as directed.
  • Read and follow all directions and warnings on this carton Do not allow contact with the eyes and mucous membranes do not bandage or apply local heat (such as heating pads) or a medicated patch to the area of use.
  • Do not use at the same time as other topical analgesics.

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)

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.

Aloe Vera Extract, Carbomer, Isopropyl Myristate, Polysorbate 80, Propylene glycol, Vitamin E, Water, 1,2 Hexanediol, Aminomethylpropanol, Butylene Glycol, Cetostearyl alcohol, Dimethicone, Edetate Disodium, Glycerin, Glycerol Mono and Dipalmitostearate, hydroxyacetophenone

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.

This label’s list of inactive ingredients names none of: lactose, wheat or gluten, colour dyes, sugars, sugar alcohols, alcohol (ethanol), aspartame (phenylalanine), gelatin, peanut oil, soy, parabens, sulfites, titanium dioxide.

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.

Same active substance, strength and form in other countries

Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.

Medicine passport: one printable page to show a pharmacist abroad

CanadaNo exact match for this strength and form

Details

Made byTrifecta Pharmaceuticals USA
Active substanceLidocaine
Used inPain, sleep, mood, epilepsy and the brain
Strength40 g/L
FormGel
RouteTopical
Packs1 BOTTLE in 1 BOX / .073 L in 1 BOTTLE · 2 BOTTLE in 1 BOX / .073 L in 1 BOTTLE
NDC69396-188

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).

Other strengths and forms

5 products are sold under this name. Grouped by form; a number on a strength means several companies make it.

Same active substance

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