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Cold Spot Point Relief by Pure Source

Dosage form: gel
Ingredients: Menthol 0.6g in 5g, METHYL SALICYLATE 0.2g in 5g
Labeler: Pure Source
NDC Code: 65121-001

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Cold Spot Point Relief Pain relieving Gel - 5 G

Active Ingredients: Menthol, methyl salicylate.

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.

pain relieving gel.

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 gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (Menthol) Menthol0.6 g  in 5 g
METHYL SALICYLATE (SALICYLIC ACID) METHYL SALICYLATE0.2 g  in 5 g
Inactive Ingredients
Ingredient NameStrength
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 
Packaging
#Item CodePackage Description
1NDC:65121-001-005 g in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34108/24/2010
Labeler - Pure Source (969241041)
Registrant - Pure Source (969241041)
Establishment
NameAddressID/FEIOperations
Pure Source969241041manufacture

 
Pure Source

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Medically reviewed on Aug 28, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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