Label: JUST CBD - CBD AND THC ULTRA RELIEF- menthol, camphor gel

  • NDC Code(s): 73647-026-04, 73647-062-04
  • Packager: Just Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 13, 2024

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

  • ACTIVE INGREDIENT

    Camphor 2%

    Menthol 6%

  • 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.

  • 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.

  • 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 and Children over 21 years:

    Apply a small amount on the affected area.
    Massage in circular motion, let set for a few seconds.
    Repeat as neccesary, but no more than 3 to 4 times daily

    Wash hands with soap and water after use.

  • OTHER SAFETY INFORMATION

    Store tightly closed in a dry place at controlled room temperature between 59°-86° f (15°-30° c). This product is intended for use by healthy adults aged 21 years & older. consult a healthcare professional prior to use of full spectrum THC. Full spectrum THC may be harmful if you are pregnant, nursing or are taking any medication or have a medical condition.

  • INACTIVE INGREDIENT

    Water (Aqua), Alcohol Denat, Propylene Glycol, Polysorbate 20, Salicylic Acid, Glycerin, Carbomer, Sodium Hydroxide, Mentha Piperita (Peppermint) Oil, Cannabidiol, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Delta-8-Tetrahydrocannabinol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Benzyl Alcohol, Sorbic Acid, FD&C Blue No.1 (CI 42090), FD&C Yellow No.5 (CI 19140), Limonene.

  • JUST CBD - CBD+THC ULTRA RELIEF GEL +1000

    JUST CBD THC 1000

  • JUST CBD - CBD+THC ULTRA RELIEF GEL +5000

    JUST CBD THC 5000

  • INGREDIENTS AND APPEARANCE
    JUST CBD - CBD AND THC ULTRA RELIEF 
    menthol, camphor gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73647-062
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL6 g  in 100 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    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)  
    .DELTA.8-TETRAHYDROCANNABINOL (UNII: B49D0HH807)  
    Product Characteristics
    ColorturquoiseScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73647-062-04113 g 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 - CBD AND THC ULTRA RELIEF 
    menthol, camphor gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73647-026
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL6 g  in 100 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)2 g  in 100 g
    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)  
    .DELTA.8-TETRAHYDROCANNABINOL (UNII: B49D0HH807)  
    Product Characteristics
    ColorturquoiseScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73647-026-04113 g 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)