Label: PROFESSIONAL THERAPY MUSCLECARE- camphor, menthol cream

  • NDC Code(s): 70039-298-08
  • Packager: Active and Innovative Inc.
  • 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 August 11, 2016

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  • PURPOSE

    FOR MUSCLE & JOINT PAIN RELIEF

  • Active Ingredietns (% by weight) Purpose

    Camphor 4%.........................Analgesic (pain relief)

    Menthol 4%...........................Analgesic (pain relief)

  • Uses:

    For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains, etc.

  • Warnings:

    For external use only.

    • Avoid getting into eyes or on mucous membranes.
    • 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 this product and consult a doctor.
    • Do not apply to wounds or damaged skin. Do not bandage tightly.
  • Keep out of reach of children.

    • Use only as directed
    • Do not use if pregnant or breastfeeding
    • If swallowed, get medical help or contact a Poison Control center right away.
  • DOSAGE & ADMINISTRATION

    Directions: Adults and children 12 years of age or older: Rub this soothing cream on the affected area not more than 3 to 4 times daily. Children under the age of 12: Do not use, consult a doctor.

  • STORAGE AND HANDLING

    Other Information: Store under normal storage conditions. Store away from children.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water/Aqua, Cetyl Alcohol, Glycol Stearate, MSM (methylsulfonylmethane), Glycerin,

    Stearyl Alcohol, Glucosamine Sulfate, Polyacrylamide (and) C13-14 Isoparaffin (and) Laureth-7, Tocopherol (Vitamin E) Acetate, Oil of Wintergreen (Methyl Salicylate), Grape Seed Oil, Sea Cucumber (Stichopus Horrens) Extract, Urea, Phenoxyethanol (and) Caprylyl Glycol (and) Sorbic Acid, Polysorbate-20, Eucalyptus Globulus Leaf Oil, Thymol, Aloe Barbadensis Leaf Juice, Chondroitin Sulfate, Magnesium Chloride

  • Professionl Therapy MuscleCare Maximum Strength Pain Relieving Ointment by Dr. Chris Oswald

    Full product label. Full product label

  • INGREDIENTS AND APPEARANCE
    PROFESSIONAL THERAPY MUSCLECARE 
    camphor, menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70039-298
    Route of AdministrationTOPICAL, CUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)40 mg  in 1 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    SORBIC ACID (UNII: X045WJ989B)  
    THYMOL (UNII: 3J50XA376E)  
    CHONDROITIN SULFATE (CHICKEN) (UNII: 7VZ9466BAB)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    WATER (UNII: 059QF0KO0R)  
    GRAPE SEED OIL (UNII: 930MLC8XGG)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    LAURETH-7 (UNII: Z95S6G8201)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    STICHOPUS SEA CUCUMBER (UNII: RO6YEJ571T)  
    (HYDROXYMETHYL)UREA (UNII: 15BY095DMS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70039-298-08115 g in 1 TUBE; Type 0: Not a Combination Product06/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34806/01/2015
    Labeler - Active and Innovative Inc. (206978079)
    Establishment
    NameAddressID/FEIBusiness Operations
    PureTek Corp.785961046manufacture(70039-298)
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