COLD SPOT POINT RELIEF - menthol aerosol, spray 
Pure Source

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Cold Spot Point Relief Pain relieving Spray - 2 oz. Spray

Active Ingredients: Menthol

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.

Keep out of reach of children. If swallowed consult physician

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.

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

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

 

Apply directly to effected area. Do not use more than four times per day.

ColdSpot Point Relief pain relieving spray. All natural ingredients.

COLD SPOT  POINT RELIEF menthol   aerosol, spray

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 65121-003 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Menthol (Menthol) Menthol 6 mL  in 60 mL

Inactive Ingredients Ingredient Name Strength water   ARNICA CORDIFOLIA FLOWER   CHONDROITIN SULFATE (BOVINE)   Citric Acid   EUCALYPTUS GLOBULUS LEAF   Glucosamine sulfate   ILEX PARAGUARIENSIS LEAF   Isopropyl Alcohol   Peppermint Oil   Dimethyl Sulfone   polysorbate 20   alcohol

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 65121-003-02 60 mL In 1 BOTTLE, SPRAY None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	08/24/2010

Labeler - Pure Source (969241041)

Registrant - Pure Source (969241041)

Establishment
Name	Address	ID/FEI	Operations
Pure Source		969241041	manufacture

Revised: 09/2010Pure Source