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
  • 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 March 7, 2023

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 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 12 years:

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

    Wash hands with soap and water after use.

  • INACTIVE INGREDIENT

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

  • JUST CBD ULTRA RELIEF GEL +1000

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  • JUST CBD ULTRA RELIEF GEL +5000

    JUST CBD ULTRA RELIEF GEL 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 not finalpart34803/14/2023
    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 not finalpart34803/14/2023
    Labeler - Just Brands LLC (113296558)