Medicine guide

Arnimax Penetrating Pain Relief Gel

30 mg/g · Gel

  • Available without prescription
Active substance
Menthol
Made by
WYNNPHARM INC.

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 · 2023-11-10

What it is

Topical Analgesic

Used for
  • Simple backache
  • Arthritis
  • Strains
  • Bruises
  • Sprains
How to take it

Apply and massage a thin layer to affected area no more than 3 to 4 times daily.

Full directions ↓
Do not take it if

If allergic to any ingredients listed in this product.

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
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

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

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

From the official label · 2023-11-10 · DailyMed

Do not take it if

if allergic to any ingredients listed in this product.

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 and massage a thin layer to affected area no more than 3 to 4 times daily.
  • Wash hands with soap and water after applying. Ask a doctor. Children under 12:

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

Stop and get help if

  • Condition worsens
  • Condition persists for more than 7 days or clears up and occurs again within a few days.

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

Other warnings

  • For external use only.
  • Do not use if allergic to any ingredients listed in this product.
  • When using this product
  • Use only as direcred
  • Avoid contact with eyes and mucous membranes
  • Do not apply directly to wounds or broken skin
  • Do not bandage tightly or use a heating pad. Stop use and ask a doctor if
  • Condition persists for more than 7 days or clears up and occurs again within a few days. If pregnant or breastfeeding, ask a health professional before use.
  • Keep out of reach of children. If swallowed, seek medical attention or contact a Poison Control Center right away.
  • Use only as direcred
  • Avoid contact with eyes and mucous membranes
  • Do not apply directly to wounds or broken skin
  • Do not bandage tightly or use a heating pad.

Quoted from the official label, section “Warnings”.

Pregnancy and breastfeeding

If pregnant or breastfeeding, ask a health professional before use.

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

Keep away from children

If swallowed, seek medical attention or contact a Poison Control Center right away.

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

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 Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Carbomer, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, GLycyrrhiza Glabra (Licorice) Extract, Hamamelis Virginiana (Witch Hazel) Extract, Hydroxyethyl Cellulose, Ilex Paraguariensis (Yerba Mate') Extract, Isopropyl Myristate, Methylsulfonulmethane (MSM), Phenoxyethanol, Propylene Glycol, Triethanolamine.

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

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.

Details

Made byWYNNPHARM INC.
Active substanceMenthol
Strength30 mg/g
FormGel
RouteTopical
Packs1 TUBE in 1 BOX / 75 g in 1 TUBE
NDC35324-274

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.