Medicine guide

Cooling Pain Relief

6 g/100mL + 3 g/100mL · Gel

  • Available without prescription
Active substance
Menthol, Camphor
Made by
SUNSET NOVELTIES, 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 · 2026-01-29

What it is

Topical Analgesic

Used for
  • Aid for temporary local relief of minor pain in muscles or joints.
How to take it

Repeat as needed, but no more than 3 to 4 times per day.

Full directions ↓
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

  • Aid for temporary local relief of minor pain in muscles or joints.

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 small amount on the affected area.
  • Massage in a circular motion until absorbed, let set for a few seconds.
  • Repeat as needed, but no more than 3 to 4 times per day.
  • Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).
  • Wash hands with soap and water after use.
  • Children under 12 years of age 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 or use with a heating pad
  • Avoid contact with eyes and mucous membranes Do not apply to wounds or damaged, broken, or irritated skin A transient burning sensation or redness may occur upon application but generally disappears in several days
  • If you experience an allergic reaction, discontinue use, and consult a physician Do not expose the area treated with product to heat or direct sunlight.

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”.

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), Alcohol Denat, Propylene Glycol, Polysorbate 20, Carbomer, Sodium Hydroxide, Salicylic Acid, Glycerin, Mentha Piperita (Peppermint) Oil, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Cannabis Sativa (Hemp) Seed Oil, Benzyl Alcohol, Sorbic Acid, FD&C Blue No. 1 (CI 42090), FD&C Yellow No.5 (CI 19140).

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.

  • Colour dyesFD&C Blue No. 1 (CI 42090); FD&C Yellow No.5 (CI 19140)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.

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 (2)

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 2 of 2

Details

Made bySUNSET NOVELTIES, INC
Active substanceMenthol, Camphor
Strength6 g/100mL + 3 g/100mL
FormGel
RouteTopical
Packs59 mL in 1 TUBE · 118 mL in 1 TUBE · 236 mL in 1 TUBE
NDC72937-629
NDC72937-630

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

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

  • Gel2 products
    • 6 g/100mL + 3 g/100mL2

      6 g/100mL + 3 g/100mL · 2 companies

  • Cream1 products

Same active substance

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