Label: KANGAROO CBD HEATING PAIN RELIEF- methyl salicylate, menthol cream

  • NDC Code(s): 72937-118-02, 72937-118-04, 72937-118-08, 72937-118-16
  • Packager: SUNSET NOVELTIES, 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 December 2, 2022

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.

  • 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

    A transient burning sensation or redness may occur upon application but generally disappears in several days.
    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.

  • 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.

  • 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.

  • DIRECTIONS:

    Adults an childre over 12 years of age: apply a thin layer to affected areaand rub gently no more than 3 to 4 times daily.

    Wash hands with soap and water after use.

    children undre 12 years of age; do not use unless directed by a doctor/physician.

    Store at room temperature 15°C - 30°C.

  • INACTIVE INGREDIENT

    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 #6 (CI 15985).

  • KANGAROO CBD HEATING PAIN RELIEF CREAM 2 oz

    KANGAROO HEATING PAIN RELIEF

  • KANGAROO CBD HEATING PAIN RELIEF CREAM 4 oz

    KANGAROO HEATING PAIN RELIEF 4

  • KANGAROO CBD HEATING PAIN RELIEF CREAM 8 oz

    KANGAROO HEATING PAIN RELIEF 8

  • KANGAROO CBD HEATING PAIN RELIEF CREAM 16 oz

    KANGAROO HEATING PAIN RELIEF 16

  • INGREDIENTS AND APPEARANCE
    KANGAROO CBD HEATING PAIN RELIEF 
    methyl salicylate, menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-118
    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)  
    AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
    WATER (UNII: 059QF0KO0R)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    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:72937-118-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product11/29/2022
    2NDC:72937-118-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product11/29/2022
    3NDC:72937-118-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product11/29/2022
    4NDC:72937-118-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product11/29/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34811/29/2022
    Labeler - SUNSET NOVELTIES, INC (067218145)