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 April 23, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES:
- WARNINGS
-
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.
- STOP USE AND ASK A DOCTOR IF:
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS:
-
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.
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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 - CBD+THC ULTRA RELIEF GEL +5000
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INGREDIENTS AND APPEARANCE
JUST CBD - CBD AND THC ULTRA RELIEF
menthol, camphor gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73647-062 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 g CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 2 g in 100 g Inactive Ingredients Ingredient Name Strength 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 Color turquoise Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73647-062-04 113 g 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 - CBD AND THC ULTRA RELIEF
menthol, camphor gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73647-026 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 g CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 2 g in 100 g 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) .DELTA.8-TETRAHYDROCANNABINOL (UNII: B49D0HH807) Product Characteristics Color turquoise Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73647-026-04 113 g 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)