Label: PREFERRED PLUS ARTHRITIS CREAM- menthol topical analgesic cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated March 1, 2013

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  • Active Ingredients

    Methyl salicylate 15%

    Menthol 10%

    Capsicum oleoresin (containing capsaicin 0.025%)

  • Purpose

    Topical analgesic

  • Uses

    Uses for the temporary relief of minor aches and pains of muscles and joints associated with


    • arthritis 
    • sprains
    • strains            
    • bruises
    • simple backache

  • Warning

    For external use only

  • Ask Doctor

    • condition worsens
    • excessive burning or irritation persists  
    • pain persists for more than 7days  
    • symptoms clear up and occur again within a few days
  • If pregnant or breast feeding

    ask a health professional before use.

  • Keep out of reach of children

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

  • Directions

    • apply to the affective area and gently rub it in until fully absorbed 
    • repeat asnecessary, but not more than 3 to 4 times daily.
    • for best results use continuously for 2 to 4 weeks
    • avoid washing treated area for at least 30 minutes after application
    • unless treating hands, wash hands thoroughly with soap and water immediately after use

    Children under 12
    consult a doctor

  • Inactive ingredients

    Water, Stearic Acid, Glyceryl Stearate SE, PEG-40 Stearate, Steareth-2,
    Triethanolamine, Carbomer, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben.

  • PRINCIPAL DISPLAY PANEL

    image of carton
  • INGREDIENTS AND APPEARANCE
    PREFERRED PLUS ARTHRITIS CREAM  
    menthol topical analgesic cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61715-032
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE15 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 g
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.025 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    PEG-40 STEARATE (UNII: ECU18C66Q7)  
    STEARETH-2 (UNII: V56DFE46J5)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61715-032-0258 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/23/2001
    Labeler - Kinray (012574513)
    Registrant - Reese Pharmaceutical Co (004172052)
    Establishment
    NameAddressID/FEIBusiness Operations
    Reese Pharmaceutical Co004172052relabel(61715-032) , repack(61715-032)