JUST CBD ULTRA RELIEF- menthol, camphor gel 
Just Brands LLC

----------

73647-602-04
73647-206-04

Camphor 2%

Menthol 6%

Topical Analgesic

USE

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

For external use only.

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

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.

Ask a health professional before use.

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.

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

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)

Revised: 3/2024
Document Id: 13eef0db-b216-5628-e063-6394a90a20d4
Set id: f65327b3-9c97-58f3-e053-2995a90a3f55
Version: 2
Effective Time: 20240318
 
Just Brands LLC