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Mountain ice pain relief - Medication Information

Product NDC Code 72793-100
Drug Name

Mountain ice pain relief

Type Brand
Active Ingredients
Menthol, unspecified form 5 g/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 415975
Application Number M017
Labeler Name Mountainside Medical Equipment, Inc.
Packages
Package NDC Code Description
72793-100-01 118 ml in 1 tube (72793-100-01)
72793-100-03 946 ml in 1 bottle, pump (72793-100-03)
72793-100-04 6 ml in 1 packet (72793-100-04)
72793-100-05 99 ml in 1 bottle, with applicator (72793-100-05)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients: Menthol 5%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions: Adults and Children 2 years of age or older: Rub on the affected area evenly no more than 4 time. Children under 2 years of age: Consult with your doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Carbomer, Cinnamomum Camphora (Camphor) Bark Oil, Curcuma longa (Turmeric) Root Oil, Dimethyl Sulfone, Ethylhexylglycerin, Glucosamine HCl, Glycerin, Ilex Paraguariensis Leaf Extract, Isopropyl Alcohol, Limonene, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Phenoxyethanol, Polysorbate 20, Propanediol, Sodium Chondroitin Sulfate, Sodium Hyaluronate, Tocopheryl Acetate, Triethanolamine, Water (Aqua), Blue 1 (CI 42090).

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Temporary relief of minor aches and pains of muscles and joints associated with osteoarthritis, rheumatoid arthritis, muscle strains, and sprains

Purpose

Information about the drug product’s indications for use.
Purpose External Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Mountain Ice Pain Relief Menthol MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM ALOE VERA LEAF ARNICA MONTANA FLOWER CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE CAMPHOR OIL TURMERIC OIL DIMETHYL SULFONE ETHYLHEXYLGLYCERIN GLUCOSAMINE HYDROCHLORIDE GLYCERIN ILEX PARAGUARIENSIS LEAF ISOPROPYL ALCOHOL LIMONENE, (+)- TEA TREE OIL PHENOXYETHANOL POLYSORBATE 20 PROPANEDIOL HYALURONATE SODIUM .ALPHA.-TOCOPHEROL ACETATE TROLAMINE WATER

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package/Label Principal Display Panel – Tube Label Arthritis Pain Relieving Gel MOUNTAIN ICE Tumeric, Glucosamine, Chondroitin, Methylsulfonylmethane (MSM), Camphor, Menthol 5%, Arnica Montana, Aloe Vera, Tea Tree Oil, Hyaluronic acid, Vitamin E, Ilex Paraguariensis Leaf Extract. 4 fl oz (118 mL) Label image-01

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out the reach of children: If accidentally swallowed seek medical attention immediately or contact Poison Control Center right away.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product: • Do not apply to wounds, damaged skin, or irritated skin. • Do not apply with other creams, ointments, sprays or liniments. • Stop use and ask a doctor if: Conditions worsen, skin irritation develops, or condition does not improve after 7 days.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only. Flammable; keep away from excessive heat or open flame. Avoid contact with eyes or mucous membranes. When using this product: • Do not apply to wounds, damaged skin, or irritated skin. • Do not apply with other creams, ointments, sprays or liniments. • Stop use and ask a doctor if: Conditions worsen, skin irritation develops, or condition does not improve after 7 days. Keep out the reach of children: If accidentally swallowed seek medical attention immediately or contact Poison Control Center right away.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API