Label: KANGAROO CBD COOLING PAIN RELIEF- menthol, camphor gel

  • NDC Code(s): 72937-062-02, 72937-062-04, 72937-062-08, 72937-062-16
  • 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

    Menthol 6%

    Camphor 2%

  • PURPOSE

    Topical Analgesic.

    Pain Relieving.

  • USES:

    Aid for temporary local relief of minor aches of muscles and joints associated with simple backache, arthritis, sprains, and strains

  • WARNINGS

    Use only as directed. For external use only. Do not bandage tightly or use with a heating pad, pack, wrap, hot water bottle or any heating element. Keep away from children, Package not child resistant. In case of accidental ingestion, contact doctor immediately.

    If prone to allergic reaction to the product consult to a doctor before using.

  • WHEN USING

    Avoid contact with eyes and mucous membranes, rashes wounds or damaged skin
    Do not apply to wounds or damaged, broken or irritated skin

    Do not apply on nose and genital area.
    If rash, redness or itchiness results; discontinue use and consult a doctor.

    If pregnant or breast-feeding ask a health professional before use.

  • DIRECTIONS:

    Adults and Children over 12 years:

    Apply a small amount on desired area.
    Massage in circular motions until absorbed
    Repeat as necessary, but no more than 3 to 4 times per day.
    Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

    Wash hands with soap and water after use.

  • STOP USE AND ASK A DOCTOR IF:

    Conditions worsen
    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.

  • KEEP OUT OF REACH OF CHILDREN

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

  • INACTIVE INGREDIENT

    Aqua, Alcohol Denat, Propylene Glycol, Salicylic Acid, Glycerin, Polysorbate 20, Carbomer, Sodium Hydroxide, Mentha Arvensis Herb Oil, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Cannabis Sativa Seed Oil, Benzyl Alcohol, Sorbic Acid, Cannabidiol, FD&C Blue. 1 Powder (CI 42090), FD&C Yellow. 5 (CI 19140).

  • KANGAROO CBD COOLING PAIN RELIEF GEL 2 oz

    KANGAROO COOLING PAIN RELIEF 2

  • KANGAROO CBD COOLING PAIN RELIEF GEL 4 oz

    KANGAROO COOLING PAIN RELIEF 4

  • KANGAROO CBD COOLING PAIN RELIEF GEL 8 oz

    KANGAROO COOLING PAIN RELIEF 8

  • KANGAROO CBD COOLING PAIN RELIEF GEL 16 OZ

    KANGAROO COOLING PAIN RELIEF 16

  • INGREDIENTS AND APPEARANCE
    KANGAROO CBD COOLING PAIN RELIEF 
    menthol, camphor gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-062
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL6 g  in 100 mL
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    THYME OIL (UNII: 2UK410MY6B)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SORBIC ACID (UNII: X045WJ989B)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    Product Characteristics
    ColorturquoiseScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72937-062-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product11/29/2022
    2NDC:72937-062-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product11/29/2022
    3NDC:72937-062-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product11/29/2022
    4NDC:72937-062-16473 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)