NATURES SUNSHINE PRODUCTS EVERFLEX TOPICAL ANALGESIC PAIN RELIEF - menthol cream 
Wasatch Product Development, LLC

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:44717-532
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)  
MENTHOL (UNII: L7T10EIP3A)  
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:44717-532-0157 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34808/13/2010
Labeler - Wasatch Product Development, LLC (962452533)
Registrant - Nature's Sunshine Products, Inc. (081832388)
Establishment
NameAddressID/FEIBusiness Operations
Wasatch Product Development, LLC962452533manufacture

Revised: 3/2011
Document Id: 05c929d2-f4fd-4b0b-8cb9-0c2f50a8610c
Set id: e002fac1-d10e-45b4-b321-75454d059315
Version: 3
Effective Time: 20110309
 
Wasatch Product Development, LLC