Label: HEATING PAIN RELIEF- methyl salicylate, menthol cream

  • NDC Code(s): 72937-180-40, 72937-180-80
  • Packager: SUNSET NOVELTIES, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 6, 2024

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

  • ACTIVE INGREDIENT

    Methyl Salicylate 18%

    Menthol 10%

  • PURPOSE

    Topical Analgesic.

  • USES:

    Aid for temporary local relief of minor pain in muscles or joints.

  • WARNINGS

    For external use only. · Ask a doctor before use if you have redness over affected area

  • WHEN USING

    Use only as directed
    Do not bandage tightly or use with a heating pad
    Avoid contact with eyes and mucous membranes
    Do not apply to wounds or damaged, broken or irritated skin
    If you experience an allergic reaction, discontinue use and consult a doctor.

    Do not expose the area treated with product to heat or direct sunlight.

  • STOP USE AND ASK A DOCTOR IF:

    Condition worsens
    Redness is present
    Irritation develops
    Symptoms persist for more than 7 days or clear up occur again within a few days

    You experience signs injury, such as pain, swelling or blistering where the product was applied.

  • 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:

    Adults and Children over 12 years

    Apply a small amount on the affected area.
    Massage in circular motion, let set for a few seconds..
    Repeat as necessary, but no more than 3 to 4 times daily.
    Wash hands with soap and water after use.

    Children under 12 years of age consult a doctor.

  • OTHER SAFETY INFORMATION

    Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Water (Aqua), Paraffinum Liquidum, Glyceryl Stearate, Stearic Acid, Cetyl Alcohol, Dimethicone, Glycereth-26, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol, Stearyl Alcohol, Triethanolamine, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Cannabidiol, FD&C Yellow No.6 (CI 15985).

  • SUNSET - HEATING PAIN RELIEF CREAM 4 oz TUBE

    heating tube 4 oz

  • SUNSET - HEATING PAIN RELIEF CREAM 8 oz TUBE

    heating 8oz

  • INGREDIENTS AND APPEARANCE
    HEATING PAIN RELIEF 
    methyl salicylate, menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-180
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL9.8 g  in 100 mL
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE17.6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    COMFREY LEAF (UNII: DG4F8T839X)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    WATER (UNII: 059QF0KO0R)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    HYDROXYPROLINE (UNII: RMB44WO89X)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Product Characteristics
    Colororange (Light Orange) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72937-180-40118 mL in 1 TUBE; Type 0: Not a Combination Product06/26/2023
    2NDC:72937-180-80236 mL in 1 TUBE; Type 0: Not a Combination Product06/26/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/25/2023
    Labeler - SUNSET NOVELTIES, INC (067218145)