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Myderm cooling menthol pain relief with 50 percent more menthol - Medication Information

Product NDC Code 72667-020
Drug Name

Myderm cooling menthol pain relief with 50 percent more menthol

Type Brand
Active Ingredients
Menthol 15.75 g/100ml
Route TOPICAL
Dosage Form SPRAY
Application Number part348
Labeler Name Inspec Solutions LLC
Packages
Package NDC Code Description
72667-020-01 89 ml in 1 bottle, spray (72667-020-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Menthol 10.5%

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.
Adults and children 2 years of age and older: Apply to affected area no more than 3 to 4 times daily. Wash hands with soap. 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 Leaf Extract Arctium Lappa Root (Burdock) Extract Arnica Montana Flower Extract Boswellia Carterii Resin Extract Calendula Officinalis Extract Camellia Sinensis Leaf Extract Camphor Carbomer FD&C Blue #1 FD&C Yellow #5 Full Spectrum Industrial Hemp Extract Glycerin Ilex Paraguariensis (Mate) Leaf Extract Isopropyl Alcohol Isopropyl Myristate Melissa Officinalis (Lemon Balm) Leaf Extract Silica Tocopheryl Acetate Triethanolamine Water

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 from minor aches and pains of muscles and joints associated with, arthritis, simple backache, strains, bruises, sprains.

Purpose

Information about the drug product’s indications for use.
Menthol 10.4% ................. Topical Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
myDerm Cooling Menthol Pain Relief with 50 Percent More Menthol Menthol FRANKINCENSE FD&C YELLOW NO. 5 GLYCERIN MELISSA OFFICINALIS LEAF TROLAMINE WATER ALOE VERA LEAF ARCTIUM LAPPA ROOT ARNICA MONTANA FLOWER ISOPROPYL MYRISTATE ILEX PARAGUARIENSIS LEAF CALENDULA OFFICINALIS FLOWER GREEN TEA LEAF CAMPHOR (NATURAL) CARBOMER 940 FD&C BLUE NO. 1 ISOPROPYL ALCOHOL SILICON DIOXIDE .ALPHA.-TOCOPHEROL ACETATE 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.
myDerm Cooling Menthol Pain Relief Spray with 50% More Menthol

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 eyes and mucous membranes., do not apply to wound or damage skin, do not bandage, do not use with heating pad or device.

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.
For external use only

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