Label: JUST CBD ULTRA RELIEF- menthol, camphor gel

  • NDC Code(s): 73647-206-04, 73647-602-04
  • Packager: Just Brands LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated March 18, 2024

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  • ACTIVE INGREDIENT

    Camphor 2%

    Menthol 6%

  • PURPOSE

    Topical Analgesic

  • USE

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

  • WARNINGS

    For external use only.

  • ASK DOCTOR

    Ask a doctore before use if you have redness over affected area

  • WHEN USING

    Use only as directed.
    Do not bandage tightly

    Do not use with heating pad, pack, wrap hot water bottle or any heating element.
    Avoid contact with eyes.
    Do not apply to wounds or damaged, broken, or irritated skin.

    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.

  • PREGNANCY 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 over 21 years:

    Apply a small amount to the affected area.
    Massage in circular motion until absorbed.
    Repeat as needed, but no more than 3 to 4 times per day.

    Wash hands with soap and water after use.

  • OTHER INFORMATION

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

    This product is intended only for use by healthy adults aged 21 years & older.

  • INACTIVE INGREDIENT

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

  • JUST CBD ULTRA RELIEF GEL +1000

    ultra relief 1000

  • JUST CBD ULTRA RELIEF GEL +5000

    ultra relief 5000

  • INGREDIENTS AND APPEARANCE
    JUST CBD ULTRA RELIEF 
    menthol, camphor gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73647-206
    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)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SORBIC ACID (UNII: X045WJ989B)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    Product Characteristics
    ColorturquoiseScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73647-206-04118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/14/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/14/2023
    JUST CBD ULTRA RELIEF 
    menthol, camphor gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73647-602
    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)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SORBIC ACID (UNII: X045WJ989B)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    Product Characteristics
    ColorturquoiseScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73647-602-04118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/14/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/14/2023
    Labeler - Just Brands LLC (113296558)
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