Medicine guide

Menthol, Camphor

10 g/100mL + 3 g/100mL · Cream

  • Available without prescription
Active substance
Menthol, Camphor
Made by
SUNSET POTENT PAIN RELIEF

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 · 2026-01-29

What it is

​Topical Analgesic

Used for
  • For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.
Warning

For external use only. · Ask a doctor before use if you have redness over affected area

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
45other products contain Menthol, Camphor — 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, sprains and strains.

From the official label · 2026-01-29 · DailyMed

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 and rub gently not more than 3 to 4 times a day. Wash hands with soap and water after use.
  • Children under 12 years of age:
  • do not use, consult a doctor.

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

Stop and get help if

Condition worsens. Redness is present. Irritation develops. Symptoms persist for more than 7 days or clear up occur again within a few days. You experience signs injury, such as pain, swelling or blistering where the product was applied.

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

Other warnings

  • For external use only. · Ask a doctor before use if you have redness over affected area
  • only as directed.
  • Do not bandage tightly.
  • Do not use with heating pad, pack, wrap, hot water bottle or any heating element.
  • In case of accidental ingestion, contact doctor immediately.
  • If prone to allergic reaction to the product, consult to a doctor before using.

Quoted from the official label, section “Warnings”.

Pregnancy and breastfeeding

If pregnant or breast – feeding Ask a health professional 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”.

Other information

Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

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

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.

Water (Aqua), Paraffinum Liquidum, Alcohol Denat, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Glycereth-26, Tocopheryl Acetate, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Cannabis Sativa (Hemp) Seed Oil, Stearyl Alcohol, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Polysorbate 20, Triethanolamine, Fragrance (Parfum), Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Benzotriazolyl Dodecyl p-Cresol, FD&C Blue No.1 (CI 42090), Linalool, Limonene, Benzyl Benzoate, Coumarin, Geraniol.

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.

  • Wheat or glutenWheat Amino AcidsMatters with coeliac disease or a wheat allergy.
  • Colour dyesFD&C Blue No.1 (CI 42090)Some people react to dyes such as tartrazine (Yellow 5) or carmine.
  • Alcohol (ethanol)Alcohol DenatMatters for children, in pregnancy, in recovery and with some medicines.
  • ParabensMethylparaben; PropylparabenPreservatives some people prefer to avoid or are sensitive to.

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.

Every version of this medicine (3)

The same active substance, strength and kind of form, from every company that sells it — with what each label lists.

Hide versions whose label lists:

Showing 3 of 3

Details

Made bySUNSET POTENT PAIN RELIEF
Active substanceMenthol, Camphor
Strength10 g/100mL + 3 g/100mL
FormCream
RouteTopical
Packs59 mL in 1 TUBE
NDC72937-627

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

9 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.