JUST CBD ULTRA RELIEF- menthol, camphor gel

JUST CBD ULTRA RELIEF by

Drug Labeling and Warnings

JUST CBD ULTRA RELIEF by is a Otc medication manufactured, distributed, or labeled by Just Brands LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

JUST CBD ULTRA RELIEF GEL +5000

INGREDIENTS AND APPEARANCE

JUST CBD ULTRA RELIEF 
menthol, camphor gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73647-206
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	6 g  in 100 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color	turquoise	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73647-206-04	118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/14/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/14/2023

JUST CBD ULTRA RELIEF 
menthol, camphor gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73647-602
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	6 g  in 100 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color	turquoise	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73647-602-04	118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/14/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/14/2023

Labeler - Just Brands LLC (113296558)