Label: MUSCLE RUB ULTRA STRENGTH CVS- camphor 4.00% menthol 10.00% methyl salicylate 30.00% spray

  • 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 December 1, 2017

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

  • Active Ingredients              Purpose

    Camphor – 4.00%                 Topical Analgesic
    Menthol – 10.00%                Topical Analgesic
    Methyl Salicylate - 30%       Topical Analgesic

  • PURPOSE

  • WarningFor external use only

    Flammable.

    • do not use while smoking or near heat or flame
    • avoid long term storage above 104oF
    • do not puncture or incinerate. Contents under pressure
    • do not store at temperature above 120oF

    When using this product

    • avoid contact with eyes and mucous membranes
    • do not apply to wounds or damages skin
    • do not bandage tightly or use with a heating pad
    • use only as directed

    Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days
    • needed for longer than 1 week

    Keep out of reach of the children

    If product is swallowed, get medical help or contact a Poison Control Center right away

  • Uses

    temporarily reliefs minor pain associated with • arthritis • simple backache •muscle strains • bruises • muscle sprains

  • Directions

    • shake well
    • adults and children 12 years of age and older: spray on affected area, not more than 3 to 4 times daily
    • children under 12 years of age: consult a doctor

  • Inactive Ingredient

    Alcohol Denat.

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    MUSCLE RUB ULTRA STRENGTH  CVS
    camphor 4.00% menthol 10.00% methyl salicylate 30.00% spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-492
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)4 g  in 100 g
    Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) Menthol10 g  in 100 g
    Methyl Salicylate (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) Methyl Salicylate30 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-492-04113 g in 1 CAN; Type 0: Not a Combination Product12/22/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34812/22/2014
    Labeler - CVS (062312574)
    Registrant - Product Quest Mfg (927768135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg927768135manufacture(59779-492)