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Myorx pain relieving - Medication Information

Product NDC Code 59088-962
Drug Name

Myorx pain relieving

Type Brand
Active Ingredients
Menthol 20 mg/ml
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 1102253,
1102257
Application Number M018
Labeler Name PureTek Corporation
Packages
Package NDC Code Description
59088-962-05 59 ml in 1 jar (59088-962-05)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Menthol 2.0%

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 and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Aloe Barbadensis (Aloe Vera) Leaf Juice, Borago Officinalis Seed Oil, Capsaicin, Carbomer, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Citric Acid, Eucalyptus Globulus Leaf Oil, Fructose, Menhaden Oil, Methyl Salicylate, Methylparaben, Phenoxyethanol, Propylene Glycol, Propylparaben, Purified Water, Squalane, Stearic Acid, Stearyl Alcohol, Tetrasodium EDTA, Tocopheryl Acetate (Vitamin E), Triethanolamine, Vitis Vinifera (Grape) Seed Oil.

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

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
MyoRx Pain Relieving Menthol ALOE VERA LEAF BORAGE SEED OIL CAPSAICIN CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) POLYOXYL 20 CETOSTEARYL ETHER CETOSTEARYL ALCOHOL CETYL ALCOHOL CITRIC ACID MONOHYDRATE EUCALYPTUS OIL FRUCTOSE HYDROGENATED MENHADEN OIL METHYL SALICYLATE METHYLPARABEN PHENOXYETHANOL PROPANEDIOL PROPYLPARABEN WATER SQUALANE STEARIC ACID STEARYL ALCOHOL EDETATE SODIUM .ALPHA.-TOCOPHEROL ACETATE, DL- TROLAMINE GRAPE SEED OIL MENTHOL MENTHOL

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.
Label image description

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not apply on wounds or damaged skin bandage tightly

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 of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days

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 avoid contact with the eyes

Storage and handling

Information about safe storage and handling of the drug product.
Store at controlled room temperature 59°-86°F (15°-30°C).

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. Do not apply on wounds or damaged skin bandage tightly When using this product avoid contact with the eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days

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