COLD SPOT POINT RELIEF- menthol gel 
Pure Source

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.

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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.
carton image
COLD SPOT  POINT RELIEF
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) Menthol0.6 g  in 5 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE0.2 g  in 5 g
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
ARNICA CORDIFOLIA FLOWER (UNII: JCG1OSZ7A8)  
CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)  
Citric Acid (UNII: 2968PHW8QP)  
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
Glucosamine sulfate (UNII: 1FW7WLR731)  
Ilex Paraguariensis Leaf (UNII: 1Q953B4O4F)  
Isopropyl Alcohol (UNII: ND2M416302)  
Peppermint Oil (UNII: AV092KU4JH)  
Dimethyl Sulfone (UNII: 9H4PO4Z4FT)  
polysorbate 20 (UNII: 7T1F30V5YH)  
alcohol (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
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/FEIBusiness Operations
Pure Source969241041manufacture

Revised: 8/2010
Document Id: d9351ee3-9e8e-4325-8868-c7ccb17d3c3a
Set id: 1b2efd8c-1878-43d6-b7e5-d431852e8a10
Version: 5
Effective Time: 20100828
 
Pure Source