Label: JOINT AND MUSCLE PAIN- menthol cream 

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

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 11/13

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Menthol (5%)

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  • PURPOSE

    Topical Analgesic

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  • Uses

    Provides penetrating temporary relief for minor pain in muscles and joints associated with:

    • Backache
    • Arthritis
    • Bruises
    • Sprains
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  • Warnings

    • For external use only. Do not use with a heating pad.  Do not apply to wounds or damaged skin. Do not bandage tightly after use.
    • Avoid contact with eyes.
    • Discontinue use and consult a physician if condition worsens, or if symptoms persist more than 7 days, or clear up and occur again within a few days.
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  • Keep out of reach of children.

    If swallowed, get medical help or contact a poison control center right away.

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  • Directions

    • Adults and children over the age of 2: Apply generously to affected area.  Massage well into painful area. Repeat as necessary, but not more than 3 to 4 times daily.
    • Children under the age of 2: Do not use; consult a physician.
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  • Inactive Ingredients

    Water, Butylene Glycol, Prunus amygdalus dulcis (Sweet Almond) Oil, PEG-12 Glyceryl Distearate, Cetyl Alcohol, Glyceryl Stearate, Cyclomethicone, PEG-100 Stearate, Dimethicone, Aloe barbadensis Leaf Extract, Ehtylhexylglycerin, Carbomer, Caprylyl Glycol, Hexylene Glycol, Phenoxyethanol, Triethanolamine, Xanthan Gum.

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  • PRINCIPAL DISPLAY PANEL

    Shaklee

    PAIN RELIEF

    0.07 OZ. (2 g)

    Distributed by Shaklee Corporation, 4747 Willow Road, Pleasanton, CA 94588
    Item#60700 SAMPLE NOT FOR RESALE XN164A

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  • INGREDIENTS AND APPEARANCE
    JOINT AND MUSCLE PAIN 
    menthol cream
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:59899-008
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Menthol (Menthol) Menthol 5 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    BUTYLENE GLYCOL  
    ALMOND OIL  
    CETYL ALCOHOL  
    GLYCERYL MONOSTEARATE  
    CYCLOMETHICONE  
    PEG-100 STEARATE  
    DIMETHICONE  
    ALOE VERA LEAF  
    ETHYLHEXYLGLYCERIN  
    CAPRYLYL GLYCOL  
    HEXYLENE GLYCOL  
    PHENOXYETHANOL  
    TROLAMINE  
    XANTHAN GUM  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:59899-008-01 2 g in 1 PACKET
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 11/11/2013
    Labeler - Shaklee Corporation (020284076)
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