NATURES SUNSHINE PRODUCTS EVERFLEX TOPICAL ANALGESIC PAIN RELIEF - menthol cream 
Natures Sunshine Products, Inc.

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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Everflex Topical Analgesic Pain Relief Cream

Active Ingredients                         Purpose

Menthol 1.25%                              Topical analgesic

Everflex pain relief cream provides temporary relief from aching joints and the surrounding tissues. Ever flex contains a proprietary blend of esterified fatty acids which is clinically proven to provide arthritis relief, plus MSM.


-Keep out of reach of children


-If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of product and consult a physician

-Do not apply to wounds or damaged skin

-Do not bandage tightly


Other Information: Store in a cool, dry place.

-For external use only

-Avoid contact with eyes

Directions for use: Massage Everflex into painful areas 3 to 4 times per day.

Inactive Ingredients: Water, Glyceryl Stearate, Glycerin, Methylsulfonylmethane (MSM), Cetyl Myristoleate, Olea Europaea (Olive) Fruit Oil, Cetyl Myristate, Lecithin, Menthol, Tocopheryl Acetate, Benzyl Alcohol, Phenoxyethanol, Carbomber, PEG-100 Stearate, Potassium Hydroxide, Cetyl Palmitoleate, Cetyl Oleate, Cetyl Palmitate, Cetyl Laurate, Methylparaben, Propylparaben, Ethylparaben, Butylparaben, Isobutylparaben.

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Everflex Topical Analgesic Pain Relief Cream with MSM

2 Oz. (57 Grams)



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NATURES SUNSHINE PRODUCTS  EVERFLEX TOPICAL ANALGESIC PAIN RELIEF
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61582-532
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.25 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
CETYL MYRISTATE (UNII: 7OPL833Q4D)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PEG-100 STEARATE (UNII: YD01N1999R)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
CETYL PALMITOLEATE (UNII: 962I97113K)  
CETYL OLEATE (UNII: 78K2L26L8N)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
ETHYLPARABEN (UNII: 14255EXE39)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61582-532-0157 g in 1 JAR; Type 0: Not a Combination Product08/13/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34808/13/2010
Labeler - Natures Sunshine Products, Inc. (809048960)
Registrant - Wasatch Product Development, LLC (962452533)
Establishment
NameAddressID/FEIBusiness Operations
Wasatch Product Development, LLC962452533manufacture(61582-532)

Revised: 5/2017
Document Id: d04904d2-471a-49b1-ac42-e4719b448760
Set id: db73d2c8-9765-4848-823b-3311aba8e1fc
Version: 9
Effective Time: 20170522
 
Natures Sunshine Products, Inc.