Skip to Content

Gout Reliever Synergy

Medically reviewed on October 24, 2016

Dosage form: oil
Ingredients: MENTHOL 20mg in 500mg
Labeler: PHYTOPIA CO., LTD.
NDC Code: 70470-1113

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.

Drug facts

Methyl salicylate 50mg

Menthol 20mg

Analgesic in the treatment of gout pain. Helps relieve the condition of pain and stiffness.

Drug facts

Methyl salicylate 50mg

Menthol 20mg

Analgesic in the treatment of gout pain. Helps relieve the condition of pain and stiffness.

Dosage and Usage

Adults 5ml maximum per day

Apply on skin and gentle massage around painful area.

Dosage and Usage

Adults 5ml maximum per day

Apply on skin and gentle massage around painful area.

Other ingredients

Arnica montana, peppermint, olive oil, grapefruit oil, eucalyptus oil, matricaria recutita, juniper berry oil, borage oil

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children. Protect this product from excessive heat and direct sun.

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children. Protect this product from excessive heat and direct sun.

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children. Protect this product from excessive heat and direct sun.

GOUT RELIEVER SYNERGY 
gout reliever synergy oil
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70470-1113
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL20 mg  in 500 mg
Inactive Ingredients
Ingredient NameStrength
JUNIPER BERRY OIL 
MATRICARIA RECUTITA 
ARNICA MONTANA 
BORAGE OIL 
GAULTHERIA PROCUMBENS LEAF 
PEPPERMINT OIL 
GRAPEFRUIT OIL 
EUCALYPTUS OIL 
OLIVE OIL 
Product Characteristics
Colorbrown (Bottle Color) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:70470-1113-5500 mg in 1 BOTTLE, GLASS
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34604/01/2016
Labeler - PHYTOPIA CO., LTD. (656940504)
Registrant - PHYTOPIA CO., LTD. (656940504)
Establishment
NameAddressID/FEIOperations
PHYTOPIA CO., LTD.656940504manufacture(70470-1113)

 
PHYTOPIA CO., LTD.

Further information

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

Hide