FDA Label for Cold Spot Point Relief
View Indications, Usage & Precautions
Cold Spot Point Relief Product Label
The following document was submitted to the FDA by the labeler of this product Fabrication Enterprises. 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 Ingredients: Menthol, methyl salicylate
Inactive Ingredient
Inactive Ingredients: deionized water, arnica, chondroitin sulfate, citirc acid, euclayptus oil, glucosamine sulfate, ilex paraguariesis leaf, isopropyl alcohol, peppermint oil, dimethyl sulfone, polysorbate-20, SD alcohol 40B.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed consult physician
Warnings
Warnings Section: For external use only, avoid contact with eyes, do not apply to open wounds or damaged skin, if symptoms persist for more than seven days discontinue use and consult physician, keep out of reach of children and if swallowed consult physician, do not bandage tightly.
Otc - Purpose
pain relieving gel.
Indications & Usage
Use: For
temporary relief of minor aches and pains of the muscles and joints
associated with simple backache, arthritis, bruises, strains and/or
sprains.
Dosage & Administration
Apply directly to effected area. Do not use more than four times per day.
Package Label.Principal Display Panel
ColdSpot Point Relief Pain Relieving spray, all natural ingredients.
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