FDA Label for Myderm Pro Freeze Cooling Menthol Pain Relief Roll-on
View Indications, Usage & Precautions
Myderm Pro Freeze Cooling Menthol Pain Relief Roll-on Product Label
The following document was submitted to the FDA by the labeler of this product Inspec Solutions. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredient
Menthol 6%
Otc - When Using
When using this product avoid contacts with the eyes or mucous membranes. do not apply to wounds or damaged skin. do not apply to irritated skin. do not bandage. wash hands after use with cool water. do not use with heating pad or device.
Otc - Purpose
Menthol 6%------------------------------------------------------------Topical Analgesic
Warnings
For external use only.
Otc - Stop Use
Stop use and ask doctor if condition worsens, or if symtoms persist for more than 7 days, or clean up and reoccur again within a few days.
Otc - Keep Out Of Reach Of Children
keep out of reach of children if swallowed,get medical help or contact a poson Control Center Immediately.
Inactive Ingredient
Inactive Ingredient
Aloe Barbadensis Leaf Juice
Arctium Lappa Root 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
Glycerin
Isopropyl Alcohol
Isopropyl Myristate
llex Paraguariensis Leaf Extract
Melissa Officinalis Leaf Extract
Phenoxyethanol
Silicon dioxide
Tocopheryl Acetate
Triethanolamine
Water
Dosage & Administration
Direction: Apply to affectered area not more that 3 to 4 times daily.
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