Label: NATURES SUNSHINE PRODUCTS EVERFLEX TOPICAL ANALGESIC PAIN RELIEF- menthol cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 Label Information

Updated May 22, 2017

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  • ACTIVE INGREDIENT

    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.

    image of back label

  • PRINCIPAL DISPLAY PANEL



    Everflex Topical Analgesic Pain Relief Cream with MSM

    2 Oz. (57 Grams)



    Image of front label

  • INGREDIENTS AND APPEARANCE
    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)
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